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Newborn with ambigous genitalia and refractory convulsions: Case report of XLAG syndrome
X-linked lissencephaly, absent corpus callosum, and epilepsy of neonatal onset with ambiguous genitalia are the classical features of XLAG syndrome and as of now very few cases have been reported in the literature. In this study, we present the case of XLAG syndrome who presented in neonatal period...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586584/ https://www.ncbi.nlm.nih.gov/pubmed/33110888 http://dx.doi.org/10.4103/jfmpc.jfmpc_922_20 |