Update on Progeria, or Hutchinson-Gilford Progeria Syndrome
sufferer Hayley Ohines.
Autosomal dominant dilated cardiomyopathy with conduction system disease * Autosomal dominant and recessive Emery Dreifuss Muscular Dystrophy * Limb girdle muscular dystrophy type 1B with atrioventricular conduction disturbances * Autosomal recessive type 2 Charcot Marie Tooth * Mandibuloacral dysplasia * Dunnigan-type familial partial lypodystrophy * Generalized lipoatrophy, insulin-resistant diabetes, leukomelanodermic papules, liver steatosis and cardiomyopathy * Hutchinson-Gilford progeria syndrome
* Atypical Werner syndrome * Restrictive Dermopathy
Around this time, his youngest sister, Amy, died of Hutchinson-Gilford Progeria Syndrome
, a disease that prematurely ages its victim and leads to an early death.
Sevy" has a probable diagnosis of Hutchinson-Gilford progeria syndrome
(rapid aging syndrome, a rare genetic disorder).