Hypoparathyroidism in an Egyptian child with Hutchinson-Gilford progeria syndrome: a case report

INTRODUCTION: Hutchinson-Gilford progeria syndrome is a rare genetic disorder. It is reported to be present in one in eight million and is characterized by severe growth failure, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, early atherosclerosis and facial fe...

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Detaylı Bibliyografya
Asıl Yazarlar: Kalil, Kotb Abbass Metwalley, Fargalley, Hekma Saad
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2012
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3269350/
https://ncbi.nlm.nih.gov/pubmed/22251708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-6-17
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