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...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Federation of Turkish Pathology Societies
2019-05-01
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| Col·lecció: | Türk Patoloji Dergisi |
| Matèries: | |
| Accés en línia: |
http://www.turkjpath.org/pdf.php3?id=1828
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