A rare case of heterotaxy syndrome with agenesis of the head and uncinate process of the pancreas
Küçük Resim Yok
Tarih
2016
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Allied Acad
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Heterotaxy syndrome is a rare complex syndrome characterized by cardiac and extra cardiac congenital malformations. The syndrome is divided into two main groups; right isomerism (Ivemark syndrome, asplenia) and left isomerism (polysplenia syndrome). Here we report a polysplenia syndrome with agenesis of head and uncinate process of the pancreas in a 52 year old woman who admitted to our clinic with complaints of weakness, lumbalgia, abdominal distention and constipation.
Açıklama
Anahtar Kelimeler
Polysplenia, Heterotaxy Syndrome, Agenesis of Pancreatic Head, Pancreas
Kaynak
Biomedical Research-India
WoS Q Değeri
Q4
Scopus Q Değeri
N/A
Cilt
27
Sayı
3
