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MURCS association with situs inversus totalis: Expanding the spectrum or a novel disorder

We are reporting a female patient with a MURCS association (Müllerian duct aplasia, unilateral renal agenesis, cervico-thoracic somite fusion defects), situs inversus totalis, short stature with normal development and intelligence. We are presenting the comparison with two other patients published w...

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Detalles Bibliográficos
Publicado en:J Pediatr Genet
Autores principales: Ekbote, Alka V., Kamath, Mohan S., Danda, Sumita
Formato: Artigo
Lenguaje:Inglês
Publicado: Georg Thieme Verlag KG 2014
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5021002/
https://ncbi.nlm.nih.gov/pubmed/27625874
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-14096
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