Progeria (Hutchison-Gilford syndrome) in siblings: in an autosomal recessive pattern of inheritance.

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dc.contributor.authorRaghu, T Yen_US
dc.contributor.authorVenkatesulu, G Aen_US
dc.contributor.authorKantharaj, G Ren_US
dc.contributor.authorSuresh, Ten_US
dc.contributor.authorVeeresh, Ven_US
dc.contributor.authorHanumanthappa, Yen_US
dc.date.accessioned2009-05-28T08:05:18Z
dc.date.available2009-05-28T08:05:18Z
dc.date.issued2001-09-01en_US
dc.description.abstractProgeria is an autosomal dominant, premature aging syndrome. Six and three year old female siblings had sclerodermatous changes over the extremities, alopecia, beaked nose, prominent veins and bird-like facies. Radiological features were consistent with features of progeria. The present case highlights rarity of progeria in siblings with a possible autosomal recessive pattern.en_US
dc.description.affiliationDepartment of Skin and Sexually Transmitted Diseases, Viydyanagar Institute of Medical Sciences, Government Medical College, Bellary-583 104, Karnataka, India.en_US
dc.identifier.citationRaghu TY, Venkatesulu GA, Kantharaj GR, Suresh T, Veeresh V, Hanumanthappa Y. Progeria (Hutchison-Gilford syndrome) in siblings: in an autosomal recessive pattern of inheritance. Indian Journal of Dermatology, Venereology and Leprology. 2001 Sep-Oct; 67(5): 261-2en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/52089
dc.language.isoengen_US
dc.source.urihttps://www.ijdvl.comen_US
dc.titleProgeria (Hutchison-Gilford syndrome) in siblings: in an autosomal recessive pattern of inheritance.en_US
dc.typeJournal Articleen_US
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