Complete urorectal septal malformation with left hemimelia in a neonate: an uncommon association
نویسندگان
چکیده
منابع مشابه
Urorectal septum malformation sequence in a newborn with VACTERL association.
Urorectal septum malformation sequence (URSMS) is an extremely rare anomaly, consists of multiple system anomalies including ambiguous genitalia, absence of a perineal opening, an imperforate anus, and urological, colonic and lumbosacral defects. We describe a newborn with characteristic URSMS who also had features of congenital varus deformity of leg, polydactyly, tracheo-oesophageal fistula, ...
متن کاملConcordant partial urorectal septum malformation sequence in monozygotic twins.
The urorectal septum malformation (URSM) sequence is defined as the absence of the perineal and anal opening in association with ambiguous genitalia and urogenital, colonic, and lumbosacral anomalies. The URSM sequence is usually lethal in the newborn period due to pulmonary hypoplasia resulting fromsevere oligohydramnios. The abnormalities of this condition are though to arise early in develop...
متن کاملAn Uncommon Feature of Chronic Granulomatous Disease in a Neonate
Chronic Granulomatous Disease (CGD) represents recurrent life-threatening bacterial and fungal infections and granuloma formation with a high mortality rate. CGD's sign and symptoms usually appear in infancy and children before the age of five; therefore, its presentation in neonatal period with some uncommon features may be easily overlooked. Here we describe a case of CGD in a 24-day-old boy,...
متن کاملMassive Bleeding from Left Colonic Arteriovenous Malformation in a Young Patient with Ventricular Septal Defect
Arteriovenous malformation of the gut is well known to have been an important bleeding focus in past ages. We report a young Korean male patient, who had been known to have ventricular septal defect, presenting massive lower gastrointestinal bleeding from an arteriovenous malformation involving a long segment of the left colon. Angiographic, gross and histologic findings are presented and the l...
متن کاملThe prune belly syndrome in a female foetus with urorectal septum malformation sequence: a case report on a rare entity with an unusual association.
The prune belly syndrome is a rare congenital anomaly which is characterized by the triad of an absent or a deficient development of the abdominal muscle, bilateral cryptorchidism and an anomalous urinary tract. In its full form, this condition occurs only in males. However, a similar condition occurs in females in the absence of cryptorchidism. On the other hand, the urorectal septum malformat...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2021
ISSN: 1757-790X
DOI: 10.1136/bcr-2020-241423