Journal Basic Info
- Impact Factor: 1.809**
- H-Index: 6
- ISSN: 2474-1655
- DOI: 10.25107/2474-1655
Major Scope
- Anesthesiology and Pain Medicine
- Physiology
- Allergy & Immunology
- Veterinary Sciences
- Otolaryngology
- Pharmacology and Therapeutics
- Vascular Medicine
- Child Birth
Abstract
Citation: Ann Clin Case Rep. 2019;4(1):1606.DOI: 10.25107/2474-1655.1606
Case Report of an Iraqi Patient with Progeria and Pulmonary Fibrosis
Faiq IG, Ameer SH, Jasmine AH and Farah JM
Department of Medicine, University of Baghdad, Iraq
Department of Neurology, Baghdad Teaching Hospital, Iraq
Department of Medicine, AlNahrain University, Iraq
Department of Medicine, Almostansrea University, Iraq
*Correspondance to: Jasmine AH
PDF Full Text Case Report | Open Access
Abstract:
Hutchinson-Gilford progeria syndrome is a rare genetic disorder. It was reported in literature as one case in eight million and causes growth retardation, hair loss, lipodystrophy, scleroderma-like skin and pulmonary changes, osteolysis, early atherosclerosis and facial features that resemble those of older people. Here, we report the case of a 16-year-old Iraqi girl with Hutchinson-Gilford progeria syndrome and pulmonary Fibrosis.
Keywords:
Cite the Article:
Faiq IG, Ameer SH, Jasmine AH, Farah JM. Case Report of an Iraqi Patient with Progeria and Pulmonary Fibrosis. Ann Clin Case Rep. 2019; 4: 1606.
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