Download scientific diagram | Small hands characteristic of Prader-Willi syndrome. from publication: Severe Short Stature in an Adolescent Male with Prader-Willi Syndrome and Congenital Adrenal Hyperplasia: A Therapeutic Conundrum | Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency results in excess androgen production which can lead to early epiphyseal fusion and short stature. Prader-Willi syndrome (PWS) is a genetic disorder resulting from a defect on chromosome 15 due to paternal | Prader-Willi Syndrome, Congenital Adrenal Hyperplasia and Adolescents | ResearchGate, the professional network for scientists.
Ophthalmologic Features of Prader-Willi Syndrome Journal of Pediatric Ophthalmology & Strabismus
Genomic CNV table. List of all CNVs identified in four samples
Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules - Journal of the American Academy of Child & Adolescent Psychiatry
Social Skills and Prader-Willi Syndrome
Identification of candidate genes on 7q by mapping CDRs by SNP-A
Identification of candidate genes on 7q by mapping CDRs by SNP-A
Possibility of early diagnosis in a fetus affected by Prader‑Willi syndrome with maternal hetero‑UPD15: A lesson to be learned
Genomic CNV table. List of all CNVs identified in four samples
J.B. QUINTOS Professor of Pediatrics, Clinician Educator