C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child

المؤلفون المشاركون

Shawqi, Rabah M.
Jamal, Radwah

المصدر

The Egyptian Journal of Medical Human Genetics

العدد

المجلد 18، العدد 1 (31 يناير/كانون الثاني 2017)، ص ص. 93-97، 5ص.

الناشر

الجمعية المصرية للأمراض الوراثية

تاريخ النشر

2017-01-31

دولة النشر

مصر

عدد الصفحات

5

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

We report a 2.5 year old female child, third in order of birth of healthy non consanguineous Egyptian parents with C syndrome.

The patient had moderate mental retardation, trigonocephaly, protruding forehead, low anterior hair line, wide upslanted palpebral fissures, depressed nasal bridge, broad nose, high arched palate, microretrognathia, low set ears, short neck, scoliosis, hypertrichosis over the back, talipes equinovarus as well as interatrial septal defect.

The patient had in addition chalazion in left lower eyelid as well as bilateral Bitot’s spots most probably due to vitamin A deficiency.

MRI brain revealed agenesis of the corpus callosum.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Shawqi, Rabah M.& Jamal, Radwah. 2017. C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child. The Egyptian Journal of Medical Human Genetics،Vol. 18, no. 1, pp.93-97.
https://search.emarefa.net/detail/BIM-777820

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Shawqi, Rabah M.& Jamal, Radwah. C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child. The Egyptian Journal of Medical Human Genetics Vol. 18, no. 1 (Jan. 2017), pp.93-97.
https://search.emarefa.net/detail/BIM-777820

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Shawqi, Rabah M.& Jamal, Radwah. C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child. The Egyptian Journal of Medical Human Genetics. 2017. Vol. 18, no. 1, pp.93-97.
https://search.emarefa.net/detail/BIM-777820

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 96-97

رقم السجل

BIM-777820