Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2177924 | Egyptian Journal of Medical Human Genetics | 2016 | 4 Pages |
Abstract
We report a 4.5 year old female child with the classical triad of Meier–Gorlin syndrome (microtia, absent patella and short stature) with normal mentality. She had small triangular face, long peaked nose, high nasal bridge, bilateral low set very small ears (microtia), retromicrognathia, high arched palate, maxillary hypoplasia, decayed teeth, and bilateral partial syndactyly between 2nd and 3rd toes. Our patient had a gastroesophageal reflux, renal stones, hydronephrosis and hypoplastic labia majora and minora with clitromegaly.
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Authors
Rabah M. Shawky, Radwa Gamal,