Rare Genetic Disorders

Phelan-McDermid Syndrome, Cri du Chat, Angelman's Syndrome
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13 chromosomal disorders you may not have heard of | You've heard of Downs… Rare Genetic Disorders, Rare Disorders, Neurological Disorders, Genomic Imprinting, Patau Syndrome, Chromosomal Disorders, Different Types Of Autism, Life Science Resources, Angelman Syndrome
Resources
13 chromosomal disorders you may not have heard of | You've heard of Downs…
ultimate grant and program guide to special needs Special Needs Resources, Special Needs Mom, Special Needs Kids, Rett Syndrome, Developmental Delays, Autism Resources, Caregiver Resources, Adoptive Parents, Sensory Processing Disorder
Babysitting Children with Special Needs
ultimate grant and program guide to special needs
Mikey's Place
Mikey's Place
A database of chromosomal disorders, created and maintained by parents (pretty cool!) Unique home page Chromosomal Abnormalities, Digeorge Syndrome, Defiant Disorder, Biology Labs, Lab Activities, Learning Difficulties, Genetic Disorders
Unique The Rare Chromosome Disorder Support Group
A database of chromosomal disorders, created and maintained by parents (pretty cool!) Unique home page
Spread the Word about 22q!! Genetic Diseases, Language Delay, Speech And Language, 22q Deletion, Oppositional Defiant Disorder, Congenital Heart Defect
Spread the Word about 22q!
Spread the Word about 22q!!
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22 Cat Eye Syndrome, Phelan Mcdermid, Rare Disease, Chromosome
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Report: "UNC researchers hoping to cure rare genetic disorder" ...Angelman Syndrome Autism Spectrum Disorder, Medical Center, Unc, Genetics, Severe
UNC researchers hoping to cure rare genetic disorder
Report: "UNC researchers hoping to cure rare genetic disorder" ...Angelman Syndrome
Beckwith-Wiedemann Syndrome is a rare genetic disorder that affects approximately 1 in 13500 people Aspergers Autism, Aspergers Syndrome, Jeans For Genes Day, Edwards Syndrome, Umbilical Hernia, Biomedical Science
asperger and beckwith-wiedemann
Beckwith-Wiedemann Syndrome is a rare genetic disorder that affects approximately 1 in 13500 people
Russell-Silver Syndrome Advocate via @rssadvocate Dercums Disease, Rare Disease Awareness, Autoimmune Disease, Psoriasis Cure, Psoriasis Remedies, Mitochondrial Disease, Childhood Disease
Russell-Silver Syndrome
Russell-Silver Syndrome Advocate via @rssadvocate
Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p minus syndrome or Lejeune’s syndrome, is a rare genetic disorder due to a missing part of chromosome 5. Its name is a French term (cat-cry or call of the cat) referring to the characteristic cat-like cry of affected children Cri Du Chat Syndrome, Medical Curiosities, Genetic Counseling, Cleft Lip And Palate
Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p minus syndrome or Lejeune’s syndrome, is a rare genetic disorder due to a missing part of chromosome 5. Its name is a French term (cat-cry or call of the cat) referring to the characteristic cat-like cry of affected children
The molecular structure of IGF-1. Photos courtesy the Phelan McDermid Syndrome Foundation Growth Factor, Science News, Courtesy, Autism, Foundation, Blog
Science Blog
The molecular structure of IGF-1. Photos courtesy the Phelan McDermid Syndrome Foundation
What is The Phelan-McDermid Syndrome? | Parenting Special Needs Magazine What Is Disability, Special Needs, Special Girl, Learning Apps
What is The Phelan-McDermid Syndrome? - Parenting Special Needs Magazine
What is The Phelan-McDermid Syndrome? | Parenting Special Needs Magazine
Rare Epilepsies Network Types Of Seizures, Interactive Network, Tuberous Sclerosis, Dravet Syndrome, Epilepsy Foundation
Access the Rare Epilepsy Network Registry
Rare Epilepsies Network
PMSF - The Phelan-McDermid Syndrome Foundation Welcomes You To Our Official Site Welcome, Henry, Cloud, Therapy
PMSF - The Phelan-McDermid Syndrome Foundation Welcomes You To Our Official Site
PMSF - The Phelan-McDermid Syndrome Foundation Welcomes You To Our Official Site