Ambiguous Genitalia Associated with an Extremely Rare Syndrome: A Case Report of XLAG Syndrome and Review of the Literature

X-linked lissencephaly, absent corpus callosum, and epilepsy of neonatal onset with ambiguous genitalia comprises the XLAG syndrome and only 15 cases have been reported in literature. Due to its rarity, the exact clinical course and outcome are not known. Exact associations of this disease are also...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Türk Patoloji Dergisi
المؤلفون الرئيسيون: Brijnandan GUPTA, Prashant RAMTEKE, V K PAUL, Tarun KUMAR, Prasenjit DAS
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Federation of Turkish Pathology Societies 2019-05-01
الموضوعات:
Lissencephaly
Corpus callosum
Ambiguous genitalia
Epilepsy
Syndrome
الوصول للمادة أونلاين: http://www.turkjpath.org/pdf.php3?id=1828

الانترنت

http://www.turkjpath.org/pdf.php3?id=1828

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