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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Detalles Bibliográficos
Autores principales: Kalil, Kotb Abbass Metwalley, Fargalley, Hekma Saad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269350/
https://www.ncbi.nlm.nih.gov/pubmed/22251708
http://dx.doi.org/10.1186/1752-1947-6-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269350/
https://www.ncbi.nlm.nih.gov/pubmed/22251708
http://dx.doi.org/10.1186/1752-1947-6-17

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