Meier-gorlin syndrome : an additional Egyptian patient with gastroesophageal reflux hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly

المؤلفون المشاركون

Jamal, Radawi

المصدر

The Egyptian Journal of Medical Human Genetics

العدد

المجلد 17، العدد 4 (31 أكتوبر/تشرين الأول 2016)، ص ص. 397-400، 4ص.

الناشر

الجمعية المصرية للأمراض الوراثية

تاريخ النشر

2016-10-31

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

طب الأسنان

الملخص EN

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.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Shawqi, Rabah M.& Jamal, Radawi. 2016. Meier-gorlin syndrome : an additional Egyptian patient with gastroesophageal reflux hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly. The Egyptian Journal of Medical Human Genetics،Vol. 17, no. 4, pp.397-400.
https://search.emarefa.net/detail/BIM-737397

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Shawqi, Rabah M.& Jamal, Radawi. Meier-gorlin syndrome : an additional Egyptian patient with gastroesophageal reflux hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly. The Egyptian Journal of Medical Human Genetics Vol. 17, no. 4 (Oct. 2016), pp.397-400.
https://search.emarefa.net/detail/BIM-737397

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Shawqi, Rabah M.& Jamal, Radawi. Meier-gorlin syndrome : an additional Egyptian patient with gastroesophageal reflux hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly. The Egyptian Journal of Medical Human Genetics. 2016. Vol. 17, no. 4, pp.397-400.
https://search.emarefa.net/detail/BIM-737397

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 400

رقم السجل

BIM-737397