A Novel Case of Biliary Atresia in a Premature Neonate With 1p36 Deletion Syndrome

We describe the case of a premature male neonate diagnosed with biliary atresia who was found to have chromosome 1p36 deletion syndrome. Our patient was born prematurely, at a gestational age of 28 weeks. Pregnancy was complicated by advanced maternal age, gestational hypertension, and intrauterine...

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Detalles Bibliográficos
Autores principales: Chawla, Vonita, Anagnost, Miran Rhee, Eldemerdash, Alaa-Eldin, Reyes, Dahna, Scherr, Rebecca, Ezeanolue, Kanayo, Banfro, Francis, Alhosh, Rabea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058419/
https://www.ncbi.nlm.nih.gov/pubmed/30057923
http://dx.doi.org/10.1177/2324709618790613

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058419/
https://www.ncbi.nlm.nih.gov/pubmed/30057923
http://dx.doi.org/10.1177/2324709618790613

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