وثيقة

Thanatophoric dysplasia : a rare entity.

مؤلف
المساهمون
Kumar, Vishal., مؤلف
Jeeyar, H., مؤلف
الناشر
Oman Medical Specialty Board.
ميلادي
2011-05
اللغة
الأنجليزية
الملخص الإنجليزي
Abstract T hanatophoric dysplasia is the lethal skeletal dysplasia characterized by marked underdevelopment of the skeleton and short-limb dwarfism. The child will be having a short neck, narrow thoracic cage and protuberant abdomen. Other anatomical features include a relatively enlarged head with frontal bossing, prominent eyes, hypertelorism and the depressed nasal bridge. The diagnosis is usually made with the ultrasonography in the second trimester. In this study we report a case of this rare entity with emphasis on its anatomical features, abnormalities and clinical profile with relevant review of literature.
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Naveen, N. S., Murlimanju, B. V., Kumar, Vishal, Pulakunta, Thejodhar, & Jeeyar, H. (2011). Thanatophoric dysplasia : a rare entity. Oman Medical Journal, 26 (3), 196-197.
قالب العنصر
مقالات الدوريات

مواد أخرى لنفس الموضوع

مقالات الدوريات
1
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Somansu, Basu.
Oman Medical Specialty Board.
2009-04
مقالات الدوريات
0
0
Gowri, Vaidyanathan.
Oman Medical Specialty Board.
2009-01