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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Main Authors: Brijnandan GUPTA (Author), Prashant RAMTEKE (Author), V K PAUL (Author), Tarun KUMAR (Author), Prasenjit DAS (Author)
Format: Book
Published: Federation of Turkish Pathology Societies, 2019-05-01T00:00:00Z.
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100 1 0 |a Brijnandan GUPTA  |e author 
700 1 0 |a Prashant RAMTEKE  |e author 
700 1 0 |a V K PAUL  |e author 
700 1 0 |a Tarun KUMAR  |e author 
700 1 0 |a Prasenjit DAS  |e author 
245 0 0 |a Ambiguous Genitalia Associated with an Extremely Rare Syndrome: A Case Report of XLAG Syndrome and Review of the Literature 
260 |b Federation of Turkish Pathology Societies,   |c 2019-05-01T00:00:00Z. 
500 |a 1018-5615 
500 |a 1309-5730 
500 |a 10.5146/tjpath.2017.01391 
520 |a 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 elusive. Hereby we are reporting this extremely rare entity and we searched the English literature extensively to get consolidated knowledge regarding this entity that would help the readers. Pre-natal radiological work-up can detect these malformations, which should be followed by medical termination, counseling and karyotyping. Till date the longest survival noted was 4 years only. 
546 |a EN 
690 |a Lissencephaly 
690 |a Corpus callosum 
690 |a Ambiguous genitalia 
690 |a Epilepsy 
690 |a Syndrome 
690 |a Pathology 
690 |a RB1-214 
655 7 |a article  |2 local 
786 0 |n Türk Patoloji Dergisi, Vol 35, Iss 2, Pp 162-165 (2019) 
787 0 |n  http://www.turkjpath.org/pdf.php3?id=1828  
787 0 |n https://doaj.org/toc/1018-5615 
787 0 |n https://doaj.org/toc/1309-5730 
856 4 1 |u https://doaj.org/article/cffe4c9d031a4d8f8b9c5fce2decb737  |z Connect to this object online.