No edit summary |
No edit summary |
||
| (3 intermediate revisions by the same user not shown) | |||
| Line 4: | Line 4: | ||
==Introduction== |
==Introduction== |
||
| − | *[[ |
+ | *[[Genetic counseling: Introduction|Introduction]] |
| − | *[[ |
+ | *[[Genetic counseling: Counseling Methods|Counseling Methods]] |
| − | *[[ |
+ | *[[Genetic counseling: Counseling Theory|Counseling Theory]] |
| − | |||
==Disorder Counseling Outlines== |
==Disorder Counseling Outlines== |
||
===0-9=== |
===0-9=== |
||
| − | *[[ |
+ | *[[Genetic counseling: 1p36 Deletion Syndrome-1|1p36 Deletion Syndrome (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: 1p36 Deletion Syndrome-2|1p36 Deletion Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: 18q Deletion Syndrome|18q Deletion Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: 22q11 Deletion Syndrome|22q11 Deletion Syndrome]] |
===A=== |
===A=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Abnormal Triple Screen and Family History of PKD|Abnormal Triple Screen and Family History of PKD]] |
| − | *[[ |
+ | *[[Genetic counseling: Achondroplasia-1|Achondroplasia (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Achondroplasia-2|Achondroplasia (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Acrofacial Dysostosis Syndrome|Acrofacial Dysostosis Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Advanced Maternal Age - Amniocentesis|Advanced Maternal Age - Amniocentesis]] |
| − | *[[ |
+ | *[[Genetic counseling: Advanced Maternal Age - Chorionic Villus Sampling (CVS)|Advanced Maternal Age - Chorionic Villus Sampling (CVS) (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Advanced Maternal Age - Chorionic Villus Sampling (CVS)-2|Advanced Maternal Age - Chorionic Villus Sampling (CVS) (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Advanced Maternal Age - Chorionic Villus Sampling (CVS)-3|Advanced Maternal Age - Chorionic Villus Sampling (CVS) (outline 3)]] |
| − | *[[ |
+ | *[[Genetic counseling: Allergies and Asthma|Allergies and Asthma]] |
| − | *[[ |
+ | *[[Genetic counseling: Alpha 1 Antitrypsin Deficiency|Alpha 1 Antitrypsin Deficiency]] |
| − | *[[ |
+ | *[[Genetic counseling: Alpha Thalassemia|Alpha Thalassemia]] |
| − | *[[ |
+ | *[[Genetic counseling: Alport Syndrome|Alport Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Amyotrophic Lateral Sclerosis|Amyotrophic Lateral Sclerosis]] |
| − | *[[ |
+ | *[[Genetic counseling: Androgen Insensitivity Syndrome|Androgen Insensitivity Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Anencephaly|Anencephaly]] |
| − | *[[ |
+ | *[[Genetic counseling: Angelman Syndrome-1|Angelman Syndrome (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Angelman Syndrome-2|Angelman Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: AR Sensorineural Hearing Loss (DFNB1/Connexin 26)|AR Sensorineural Hearing Loss (DFNB1/Connexin 26)]] |
| − | *[[ |
+ | *[[Genetic counseling: Arthrogryposis|Arthrogryposis]] |
| − | *[[ |
+ | *[[Genetic counseling: Autism-1|Autism (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Autism-2|Autism (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Autism-3|Autism (outline 3)]] |
===B=== |
===B=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Balanced Robertsonian Translocation|Balanced Robertsonian Translocation]] |
| − | *[[ |
+ | *[[Genetic counseling: Balanced Translocation|Balanced Translocation]] |
| − | *[[ |
+ | *[[Genetic counseling: Bardet-Biedl Syndrome-1|Bardet-Biedl Syndrome (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Bardet-Biedl Syndrome-2|Bardet-Biedl Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Beal's Syndrome|Beal's Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Becker Muscular Dystrophy|Becker Muscular Dystrophy]] |
| − | *[[ |
+ | *[[Genetic counseling: Beckwith-Wiedemann Syndrome|Beckwith-Wiedemann Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Beta-Thalassemia|Beta-Thalassemia]] |
| − | *[[ |
+ | *[[Genetic counseling: Bloom Syndrome-1|Bloom Syndrome (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Bloom Syndrome-2|Bloom Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Breast Cancer - Ashkenazi Jew|Breast Cancer - Ashkenazi Jew]] |
===C=== |
===C=== |
||
| − | *[[ |
+ | *[[Genetic counseling: CADASIL|CADASIL]] |
| − | *[[ |
+ | *[[Genetic counseling: Canavan Disease: Heterozygote Screening|Canavan Disease: Heterozygote Screening]] |
| − | *[[ |
+ | *[[Genetic counseling: Cancer|Cancer]] |
| − | *[[ |
+ | *[[Genetic counseling: Cerebral Palsy|Cerebral Palsy]] |
| − | *[[ |
+ | *[[Genetic counseling: CHARGE Association|CHARGE Association]] |
| − | *[[ |
+ | *[[Genetic counseling: Chondrodysplasia Punctata|Chondrodysplasia Punctata]] |
| − | *[[ |
+ | *[[Genetic counseling: Chorionic Villus Sampling (CVS)|Chorionic Villus Sampling (CVS)]] |
| − | *[[ |
+ | *[[Genetic counseling: Choroid Plexus Cysts on Ultrasound|Choroid Plexus Cysts on Ultrasound]] |
| − | *[[ |
+ | *[[Genetic counseling: Classical Myotonic Dystrophy|Classical Myotonic Dystrophy]] |
| − | *[[ |
+ | *[[Genetic counseling: Cleft Lip and Palate|Cleft Lip and Palate]] |
| − | *[[ |
+ | *[[Genetic counseling: Cleft Lip - Isolated, Unilateral, Incomplete|Cleft Lip - Isolated, Unilateral, Incomplete]] |
| − | *[[ |
+ | *[[Genetic counseling: Cleft Palate - Pierre Robin Sequence-1|Cleft Lip - Isolated, Unilateral, Incomplete (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Cleft Palate - Pierre Robin Sequence-2|Cleft Lip - Isolated, Unilateral, Incomplete (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Coffin-Lowry Syndrome|Coffin-Lowry Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Colon Cancer Prophylactic Surgery|Colon Cancer Prophylactic Surgery]] |
| − | *[[ |
+ | *[[Genetic counseling: Colorectal Cancer Chemoprevention|Colorectal Cancer Chemoprevention]] |
| − | *[[ |
+ | *[[Genetic counseling: Congenital Diaphragmatic Hernia|Congenital Diaphragmatic Hernia]] |
| − | *[[ |
+ | *[[Genetic counseling: Cornelia de Lange Syndrome|Cornelia de Lange Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Cowden Syndrome|Cowden Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Craniosynostosis-1|Craniosynostosis (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Craniosynostosis-2|Craniosynostosis (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Cri-du-chat syndrome - deletion 5p|Cri-du-chat syndrome - deletion 5p]] |
| − | *[[ |
+ | *[[Genetic counseling: Cystic Fibrosis Carrier Screening-1|Cystic Fibrosis Carrier Screening (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Cystic Fibrosis Carrier Screening-2|Cystic Fibrosis Carrier Screening (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Cystic Fibrosis - Prenatal Diagnosis-1|Cystic Fibrosis - Prenatal Diagnosis (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Cystic Fibrosis - Prenatal Diagnosis-2|Cystic Fibrosis - Prenatal Diagnosis (outline 2)]] |
===D=== |
===D=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Developmental Delay and Mental Retardation|Developmental Delay and Mental Retardation (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Developmental Delay and Mental Retardation-2|Developmental Delay and Mental Retardation (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Diabetes in Pregnancy|Diabetes in Pregnancy]] |
| − | *[[ |
+ | *[[Genetic counseling: Diabetes Mellitus|Diabetes Mellitus]] |
| − | *[[ |
+ | *[[Genetic counseling: Diabetic Embryopathy|Diabetic Embryopathy]] |
| − | *[[ |
+ | *[[Genetic counseling: Down Syndrome - Trisomy 21-1|Down Syndrome - Trisomy 21 (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Down Syndrome - Trisomy 21-2|Down Syndrome - Trisomy 21 (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Duchenne Muscular Dystrophy-1|Duchenne Muscular Dystrophy (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Duchenne Muscular Dystrophy-2|Duchenne Muscular Dystrophy (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Dysmorphic Features - Developmental Delay|Dysmorphic Features - Developmental Delay]] |
| − | *[[ |
+ | *[[Genetic counseling: Dysmorphic Features - Hypotonia|Dysmorphic Features - Hypotonia]] |
===E=== |
===E=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Echogenic Bowel|Echogenic Bowel]] |
| − | *[[ |
+ | *[[Genetic counseling: Ehlers-Danlos Syndrome|Ehlers-Danlos Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Ehlers-Danlos Syndrome-2|Ehlers-Danlos Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Ehlers-Danlos Syndrome-3|Ehlers-Danlos Syndrome (outline 3)]] |
| − | *[[ |
+ | *[[Genetic counseling: Epilepsy and Seizures|Epilepsy and Seizures]] |
| − | *[[ |
+ | *[[Genetic counseling: Ewing's Sarcoma|Ewing's Sarcoma]] |
===F=== |
===F=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Fabry Disease|Fabry Disease]] |
| − | *[[ |
+ | *[[Genetic counseling: Familial Adenomatous Polyposis|Familial Adenomatous Polyposis (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Familial Adenomatous Polyposis-2|Familial Adenomatous Polyposis (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Fanconi Anemia|Fanconi Anemia]] |
| − | *[[ |
+ | *[[Genetic counseling: Fetal Alcohol Syndrome|Fetal Alcohol Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Fetal Hydantoin Syndrome|Fetal Hydantoin Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Fetal Dilantin-Keppra Syndrome|Fetal Dilantin-Keppra Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Fetal Valproate Syndrome|Fetal Valproate Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: FG Syndrome|FG Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: FG Syndrome-2|FG Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: First Trimester Screening|First Trimester Screening]] |
| − | *[[ |
+ | *[[Genetic counseling: Fragile X Syndrome|Fragile X Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Friedreich Ataxia|Friedreich Ataxia]] |
| − | *[[ |
+ | *[[Genetic counseling: Frontonasal Dysplasia - Median Cleft Face Syndrome|Frontonasal Dysplasia - Median Cleft Face Syndrome]] |
===G=== |
===G=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Galactosemia|Galactosemia (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Galactosemia-2|Galactosemia (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Gastroschisis|Gastroschisis]] |
| − | *[[ |
+ | *[[Genetic counseling: Gaucher Disease|Gaucher Disease (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Gaucher Disease-2|Gaucher Disease (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Gaucher Disease-3|Gaucher Disease (outline 3)]] |
| − | *[[ |
+ | *[[Genetic counseling: Genes and Chromosomes|Genes and Chromosomes]] |
| − | *[[ |
+ | *[[Genetic counseling: Gorlin - Nevoid Basal Cell Carcinoma Syndrome|Gorlin - Nevoid Basal Cell Carcinoma Syndrome]] |
===H=== |
===H=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Hearing loss - Unknown Cause|Hearing loss - Unknown Cause]] |
| − | *[[ |
+ | *[[Genetic counseling: Heart Defects - Isolated|Heart Defects - Isolated]] |
| − | *[[ |
+ | *[[Genetic counseling: Hemifacial Microsomia|Hemifacial Microsomia]] |
| − | *[[ |
+ | *[[Genetic counseling: Hemoglobin C|Hemoglobin C]] |
| − | *[[ |
+ | *[[Genetic counseling: Hemoglobinopathy Screening and Hemoglobin D-Punjab|Hemoglobinopathy Screening and Hemoglobin D-Punjab]] |
| − | *[[ |
+ | *[[Genetic counseling: Hemophilia and Von Willebrand Disease|Hemophilia and Von Willebrand Disease]] |
| − | *[[ |
+ | *[[Genetic counseling: Hereditary Breast Cancer - BRCA1 and BRCA2|Hereditary Breast Cancer - BRCA1 and BRCA2]] |
| − | *[[ |
+ | *[[Genetic counseling: Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) and Lobular Carcinoma In Situ (LCIS)|Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) and Lobular Carcinoma In Situ (LCIS)]] |
| − | *[[ |
+ | *[[Genetic counseling: Hereditary Nonpolyposis Colorectal Cancer (HNPCC)|Hereditary Nonpolyposis Colorectal Cancer (HNPCC)]] |
| − | *[[ |
+ | *[[Genetic counseling: Holoprosencephaly|Holoprosencephaly]] |
| − | *[[ |
+ | *[[Genetic counseling: Huntington Disease|Huntington Disease]] |
| − | *[[ |
+ | *[[Genetic counseling: Hyper-extensibility|Hyper-extensibility]] |
| − | *[[ |
+ | *[[Genetic counseling: Hypoplasia - Agenesis of the Corpus Callosum|Hypoplasia - Agenesis of the Corpus Callosum]] |
| − | *[[ |
+ | *[[Genetic counseling: Hypotonia - Developmental Delay|Hypotonia - Developmental Delay]] |
===I=== |
===I=== |
||
| − | *[[ |
+ | *[[Genetic counseling: HIgA Nephropathy|IgA Nephropathy]] |
| − | *[[ |
+ | *[[Genetic counseling: Incontinence|Incontinence]] |
| − | *[[ |
+ | *[[Genetic counseling: Infertility|Infertility]] |
===J=== |
===J=== |
||
===K=== |
===K=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Keratoconus|Keratoconus]] |
| − | *[[ |
+ | *[[Genetic counseling: Klinefelter Syndrome|Klinefelter Syndrome]] |
===L=== |
===L=== |
||
| − | * [[ |
+ | * [[Genetic counseling: Lhermitte-Duclos disease|Lhermitte-Duclos disease]] {{stage short|00%|November 8, 2005}} |
| − | *[[ |
+ | *[[Genetic counseling: Lupron Exposure|Lupron Exposure]] |
===M=== |
===M=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Marfan Syndrome|Marfan Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Maternal Serum Triple Screen|Maternal Serum Triple Screen (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Maternal Serum Triple Screen-2|Maternal Serum Triple Screen (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: McCune Albright Syndrome|McCune Albright Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Medium-chain acyl-coenzyme A dehydrogenase Deficiency|Medium-chain acyl-coenzyme A dehydrogenase Deficiency]] |
| − | *[[ |
+ | *[[Genetic counseling: Microcephaly|Microcephaly]] |
| − | *[[ |
+ | *[[Genetic counseling: Miller Syndrome|Miller Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Mosaic trisomy 21 - Transient Myleoproliferative Syndrome|Mosaic trisomy 21 - Transient Myleoproliferative Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Mucopolysacharidosis (MPS)|Mucopolysacharidosis (MPS)]] |
| − | *[[ |
+ | *[[Genetic counseling: Multiple Pregnancy Loss|Multiple Pregnancy Loss]] |
===N=== |
===N=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Nager Syndrome|Nager Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Neural Tube Defects|Neural Tube Defects]] |
| − | *[[ |
+ | *[[Genetic counseling: Neurofibromatosis - Type 1|Neurofibromatosis - Type 1 (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Neurofibromatosis - Type 1-2|Neurofibromatosis - Type 1 (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Neurofibromatosis - Type 1-3|Neurofibromatosis - Type 1 (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Neurofibromatosis - Type 2|Neurofibromatosis - Type 2]] |
| − | *[[ |
+ | *[[Genetic counseling: Niemann-Pick Disease|Niemann-Pick Disease (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Niemann-Pick Disease-2|Niemann-Pick Disease (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Noonan Syndrome|Noonan Syndrome]] |
===O=== |
===O=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Oculo-Auriculo-Vertebral Spectrum|Oculo-Auriculo-Vertebral Spectrum]] |
| − | *[[ |
+ | *[[Genetic counseling: Opitz BBB - G Syndrome|Opitz BBB - G Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Oral-Facial-Digital Syndrome - Type 1|Oral-Facial-Digital Syndrome - Type 1]] |
| − | *[[ |
+ | *[[Genetic counseling: Osteogenesis Imperfecta (OI)|Osteogenesis Imperfecta (OI)]] |
| − | *[[ |
+ | *[[Genetic counseling: Osteosarcoma and Li-Fraumeni Syndrome|Osteosarcoma and Li-Fraumeni Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Ovarian Cancer|Ovarian Cancer]] |
===P=== |
===P=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Pallister-Killian Syndrome|Pallister-Killian Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Pancreatic Cancer|Pancreatic Cancer]] |
| − | *[[ |
+ | *[[Genetic counseling: Partial Trisomy 11q (q14-q21)|Partial Trisomy 11q (q14-q21)]] |
| − | *[[ |
+ | *[[Genetic counseling: Percutaneous Umbilical Blood Sampling (PUBS)|Percutaneous Umbilical Blood Sampling (PUBS)]] |
| − | *[[ |
+ | *[[Genetic counseling: Phenylketonuria (PKU)|Phenylketonuria (PKU)]] |
| − | *[[ |
+ | *[[Genetic counseling: Pierre Robin Sequence - Cleft Palate|Pierre Robin Sequence - Cleft Palate]] |
| − | *[[ |
+ | *[[Genetic counseling: Pituitary Tumor|Pituitary Tumor]] |
| − | *[[ |
+ | *[[Genetic counseling: Polycystic Kidney Disease|Polycystic Kidney Disease]] |
| − | *[[ |
+ | *[[Genetic counseling: Polydactyly and Syndactyly|Polydactyly and Syndactyly]] |
| − | *[[ |
+ | *[[Genetic counseling: Prader-Willi Syndrome - Prenatal|Prader-Willi Syndrome - Prenatal]] |
| − | *[[ |
+ | *[[Genetic counseling: Prader-Willi Syndrome-2|Prader-Willi Syndrome (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Protein S Deficiency|Protein S Deficiency]] |
===Q=== |
===Q=== |
||
===R=== |
===R=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Reciprocal Translocation|Reciprocal Translocation]] |
| − | *[[ |
+ | *[[Genetic counseling: Renal Cell Carcinoma|Renal Cell Carcinoma]] |
| − | *[[ |
+ | *[[Genetic counseling: Retinoblastoma|Retinoblastoma]] |
| − | *[[ |
+ | *[[Genetic counseling: Rett Syndrome|Rett Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Ring Chromosome 22|Ring Chromosome 22]] |
| − | *[[ |
+ | *[[Genetic counseling: Robin Sequence|Robin Sequence]] |
| − | *[[ |
+ | *[[Genetic counseling: Russell Silver Syndrome|Russell Silver Syndrome]] |
===S=== |
===S=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Smith_Magenis_Syndrome|Smith-Magenis syndrome (SMS)]] |
| − | *[[ |
+ | *[[Genetic counseling: Sanfilippo syndrome|Sanfilippo syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Scheie Syndrome|Scheie Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Seizure Medications|Seizure Medications]] |
| − | *[[ |
+ | *[[Genetic counseling: Septo-optic dysplasia|Septo-optic dysplasia]] |
| − | *[[ |
+ | *[[Genetic counseling: Short Chain Acyl-CoA Dehydrogenase (SCAD)|Short Chain Acyl-CoA Dehydrogenase (SCAD)]] |
| − | *[[ |
+ | *[[Genetic counseling: Short Stature|Short Stature]] |
| − | *[[ |
+ | *[[Genetic counseling: Sickle Cell Anemia|Sickle Cell Anemia]] |
| − | *[[ |
+ | *[[Genetic counseling: Smith-Lemli-Opitz Syndrome|Smith-Lemli-Opitz Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Sotos Syndrome|Sotos Syndrome]] |
| − | *[[ |
+ | *[[Genetic counseling: Spina Bifida|Spina Bifida]] |
| − | *[[ |
+ | *[[Genetic counseling: Spinal Muscular Atrophy (SMA1)|Spinal Muscular Atrophy (SMA1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Spontaneous Pregnancy Loss and X-chromosome Inactivation|Spontaneous Pregnancy Loss and X-chromosome Inactivation]] |
| − | *[[ |
+ | *[[Genetic counseling: Stickler Syndrome|Stickler Syndrome]] |
===T=== |
===T=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Tamoxifen - Selective Estrogen Response Modifiers (SERMS)|Tamoxifen - Selective Estrogen Response Modifiers (SERMS)]] |
| − | *[[ |
+ | *[[Genetic counseling: Tay-Sachs Disease|Tay-Sachs Disease]] |
| − | *[[ |
+ | *[[Genetic counseling: Treacher Collins|Treacher Collins]] |
| − | *[[ |
+ | *[[Genetic counseling: Trisomy 13|Trisomy 13]] |
| − | *[[ |
+ | *[[Genetic counseling: Trisomy 13 - Advanced Maternal Age - Occupational Exposures|Trisomy 13 - Advanced Maternal Age - Occupational Exposures]] |
| − | *[[ |
+ | *[[Genetic counseling: Trisomy 18|Trisomy 18]] |
| − | *[[ |
+ | *[[Genetic counseling: Tuberous Sclerosis|Tuberous Sclerosis (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Tuberous Sclerosis-2|Tuberous Sclerosis (outline 2)]] |
| − | *[[ |
+ | *[[Genetic counseling: Turner Syndrome|Turner Syndrome (outline 1)]] |
| − | *[[ |
+ | *[[Genetic counseling: Turner Syndrome-2|Turner Syndrome (outline 2)]] |
===U=== |
===U=== |
||
===V=== |
===V=== |
||
| − | *[[ |
+ | *[[Genetic counseling: VATER Association|VATER Association]] |
| − | *[[ |
+ | *[[Genetic counseling: Van Der Woude syndrome|Van Der Woude syndrome]] {{stage short|00%|February 2, 2006}} |
| − | *[[ |
+ | *[[Genetic counseling: Velo-Cardio-Facial Syndrome (VCF)|Velo-Cardio-Facial Syndrome (VCF)]] |
| − | *[[ |
+ | *[[Genetic counseling: Velopharyngeal Inadequacy (VPI)|Velopharyngeal Inadequacy (VPI)]] |
| − | *[[ |
+ | *[[Genetic counseling: Vitamin C Deficiency|Vitamin C Deficiency]] |
| − | *[[ |
+ | *[[Genetic counseling: Von Gierkes Disease (Glycogen Storage Disease Type I)|Von Gierkes Disease (Glycogen Storage Disease Type I)]] |
| − | *[[ |
+ | *[[Genetic counseling: Von Hippel-Lindau Syndrome|Von Hippel-Lindau Syndrome]] |
===W=== |
===W=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Waardenburg Syndrome|Waardenburg Syndrome]] |
===X=== |
===X=== |
||
| − | *[[ |
+ | *[[Genetic counseling: XXX Syndrome|XXX Syndrome]] |
===Y=== |
===Y=== |
||
===Z=== |
===Z=== |
||
| − | *[[ |
+ | *[[Genetic counseling: Zellweger Syndrome|Zellweger Syndrome]] |
==Sample Counseling Letters== |
==Sample Counseling Letters== |
||
Latest revision as of 17:38, 11 March 2006
Assessment |
Biopsychology |
Comparative |
Cognitive |
Developmental |
Language |
Individual differences |
Personality |
Philosophy |
Social |
Methods |
Statistics |
Clinical |
Educational |
Industrial |
Professional items |
World psychology |
Clinical: Approaches · Group therapy · Techniques · Types of problem · Areas of specialism · Taxonomies · Therapeutic issues · Modes of delivery · Model translation project · Personal experiences ·
This list was copied over from Handbook of Genetic Counseling The text provides an introduction to genetic counseling as a clinical practice and includes sample counseling outlines and letters for students of genetic counseling. Pleease add to the material if you can
Introduction
- Introduction
- Counseling Methods
- Counseling Theory
Disorder Counseling Outlines
0-9
- 1p36 Deletion Syndrome (outline 1)
- 1p36 Deletion Syndrome (outline 2)
- 18q Deletion Syndrome
- 22q11 Deletion Syndrome
A
- Abnormal Triple Screen and Family History of PKD
- Achondroplasia (outline 1)
- Achondroplasia (outline 2)
- Acrofacial Dysostosis Syndrome
- Advanced Maternal Age - Amniocentesis
- Advanced Maternal Age - Chorionic Villus Sampling (CVS) (outline 1)
- Advanced Maternal Age - Chorionic Villus Sampling (CVS) (outline 2)
- Advanced Maternal Age - Chorionic Villus Sampling (CVS) (outline 3)
- Allergies and Asthma
- Alpha 1 Antitrypsin Deficiency
- Alpha Thalassemia
- Alport Syndrome
- Amyotrophic Lateral Sclerosis
- Androgen Insensitivity Syndrome
- Anencephaly
- Angelman Syndrome (outline 1)
- Angelman Syndrome (outline 2)
- AR Sensorineural Hearing Loss (DFNB1/Connexin 26)
- Arthrogryposis
- Autism (outline 1)
- Autism (outline 2)
- Autism (outline 3)
B
- Balanced Robertsonian Translocation
- Balanced Translocation
- Bardet-Biedl Syndrome (outline 1)
- Bardet-Biedl Syndrome (outline 2)
- Beal's Syndrome
- Becker Muscular Dystrophy
- Beckwith-Wiedemann Syndrome
- Beta-Thalassemia
- Bloom Syndrome (outline 1)
- Bloom Syndrome (outline 2)
- Breast Cancer - Ashkenazi Jew
C
- CADASIL
- Canavan Disease: Heterozygote Screening
- Cancer
- Cerebral Palsy
- CHARGE Association
- Chondrodysplasia Punctata
- Chorionic Villus Sampling (CVS)
- Choroid Plexus Cysts on Ultrasound
- Classical Myotonic Dystrophy
- Cleft Lip and Palate
- Cleft Lip - Isolated, Unilateral, Incomplete
- Cleft Lip - Isolated, Unilateral, Incomplete (outline 1)
- Cleft Lip - Isolated, Unilateral, Incomplete (outline 2)
- Coffin-Lowry Syndrome
- Colon Cancer Prophylactic Surgery
- Colorectal Cancer Chemoprevention
- Congenital Diaphragmatic Hernia
- Cornelia de Lange Syndrome
- Cowden Syndrome
- Craniosynostosis (outline 1)
- Craniosynostosis (outline 2)
- Cri-du-chat syndrome - deletion 5p
- Cystic Fibrosis Carrier Screening (outline 1)
- Cystic Fibrosis Carrier Screening (outline 2)
- Cystic Fibrosis - Prenatal Diagnosis (outline 1)
- Cystic Fibrosis - Prenatal Diagnosis (outline 2)
D
- Developmental Delay and Mental Retardation (outline 1)
- Developmental Delay and Mental Retardation (outline 2)
- Diabetes in Pregnancy
- Diabetes Mellitus
- Diabetic Embryopathy
- Down Syndrome - Trisomy 21 (outline 1)
- Down Syndrome - Trisomy 21 (outline 2)
- Duchenne Muscular Dystrophy (outline 1)
- Duchenne Muscular Dystrophy (outline 2)
- Dysmorphic Features - Developmental Delay
- Dysmorphic Features - Hypotonia
E
- Echogenic Bowel
- Ehlers-Danlos Syndrome
- Ehlers-Danlos Syndrome (outline 2)
- Ehlers-Danlos Syndrome (outline 3)
- Epilepsy and Seizures
- Ewing's Sarcoma
F
- Fabry Disease
- Familial Adenomatous Polyposis (outline 1)
- Familial Adenomatous Polyposis (outline 2)
- Fanconi Anemia
- Fetal Alcohol Syndrome
- Fetal Hydantoin Syndrome
- Fetal Dilantin-Keppra Syndrome
- Fetal Valproate Syndrome
- FG Syndrome
- FG Syndrome (outline 2)
- First Trimester Screening
- Fragile X Syndrome
- Friedreich Ataxia
- Frontonasal Dysplasia - Median Cleft Face Syndrome
G
- Galactosemia (outline 1)
- Galactosemia (outline 2)
- Gastroschisis
- Gaucher Disease (outline 1)
- Gaucher Disease (outline 2)
- Gaucher Disease (outline 3)
- Genes and Chromosomes
- Gorlin - Nevoid Basal Cell Carcinoma Syndrome
H
- Hearing loss - Unknown Cause
- Heart Defects - Isolated
- Hemifacial Microsomia
- Hemoglobin C
- Hemoglobinopathy Screening and Hemoglobin D-Punjab
- Hemophilia and Von Willebrand Disease
- Hereditary Breast Cancer - BRCA1 and BRCA2
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) and Lobular Carcinoma In Situ (LCIS)
- Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
- Holoprosencephaly
- Huntington Disease
- Hyper-extensibility
- Hypoplasia - Agenesis of the Corpus Callosum
- Hypotonia - Developmental Delay
I
J
K
L
- Lhermitte-Duclos disease Template:Stage short
- Lupron Exposure
M
- Marfan Syndrome
- Maternal Serum Triple Screen (outline 1)
- Maternal Serum Triple Screen (outline 2)
- McCune Albright Syndrome
- Medium-chain acyl-coenzyme A dehydrogenase Deficiency
- Microcephaly
- Miller Syndrome
- Mosaic trisomy 21 - Transient Myleoproliferative Syndrome
- Mucopolysacharidosis (MPS)
- Multiple Pregnancy Loss
N
- Nager Syndrome
- Neural Tube Defects
- Neurofibromatosis - Type 1 (outline 1)
- Neurofibromatosis - Type 1 (outline 2)
- Neurofibromatosis - Type 1 (outline 2)
- Neurofibromatosis - Type 2
- Niemann-Pick Disease (outline 1)
- Niemann-Pick Disease (outline 2)
- Noonan Syndrome
O
- Oculo-Auriculo-Vertebral Spectrum
- Opitz BBB - G Syndrome
- Oral-Facial-Digital Syndrome - Type 1
- Osteogenesis Imperfecta (OI)
- Osteosarcoma and Li-Fraumeni Syndrome
- Ovarian Cancer
P
- Pallister-Killian Syndrome
- Pancreatic Cancer
- Partial Trisomy 11q (q14-q21)
- Percutaneous Umbilical Blood Sampling (PUBS)
- Phenylketonuria (PKU)
- Pierre Robin Sequence - Cleft Palate
- Pituitary Tumor
- Polycystic Kidney Disease
- Polydactyly and Syndactyly
- Prader-Willi Syndrome - Prenatal
- Prader-Willi Syndrome (outline 2)
- Protein S Deficiency
Q
R
- Reciprocal Translocation
- Renal Cell Carcinoma
- Retinoblastoma
- Rett Syndrome
- Ring Chromosome 22
- Robin Sequence
- Russell Silver Syndrome
S
- Smith-Magenis syndrome (SMS)
- Sanfilippo syndrome
- Scheie Syndrome
- Seizure Medications
- Septo-optic dysplasia
- Short Chain Acyl-CoA Dehydrogenase (SCAD)
- Short Stature
- Sickle Cell Anemia
- Smith-Lemli-Opitz Syndrome
- Sotos Syndrome
- Spina Bifida
- Spinal Muscular Atrophy (SMA1)
- Spontaneous Pregnancy Loss and X-chromosome Inactivation
- Stickler Syndrome
T
- Tamoxifen - Selective Estrogen Response Modifiers (SERMS)
- Tay-Sachs Disease
- Treacher Collins
- Trisomy 13
- Trisomy 13 - Advanced Maternal Age - Occupational Exposures
- Trisomy 18
- Tuberous Sclerosis (outline 1)
- Tuberous Sclerosis (outline 2)
- Turner Syndrome (outline 1)
- Turner Syndrome (outline 2)
U
V
- VATER Association
- Van Der Woude syndrome Template:Stage short
- Velo-Cardio-Facial Syndrome (VCF)
- Velopharyngeal Inadequacy (VPI)
- Vitamin C Deficiency
- Von Gierkes Disease (Glycogen Storage Disease Type I)
- Von Hippel-Lindau Syndrome
W
- Waardenburg Syndrome
X
- XXX Syndrome
Y
Z
- Zellweger Syndrome
Sample Counseling Letters
Useful Resources
Copyright
|
Much of the information for this book was originally located at http://www.genesoc.com/counseling2 . That website is now defunct and the information and content from that site is being relocated here. --Exmoron 20:47, 29 November 2005 (UTC)