Bardet-Biedl Syndrome (BBS) is a rare genetic disorder that affects multiple body systems, usually starting in early childhood. It is inherited in an autosomal...
Acanthosis Nigricans (AN) is a skin condition characterized by dark, velvety, thickened patches or plaques, typically appearing in body folds and creases. Common sites...
Pickwickian syndrome, also known as Obesity hypoventilation syndrome (OHS), is a breathing disorder that develops in some obese people. The syndromic disorder is...
Leptin Deficiency, also known as Congenital leptin deficiency (CLD), is a rare inherited disorder that causes early-onset obesity (in infants). Patients are born with...
What is Prader-Willi Syndrome?
Prader-Willi syndrome (PWS) is a rare multisystem genetic disorder affecting the metabolic, endocrine, and neurologic systems due to abnormalities on chromosome...