Waardenburg syndrome presenting with constipation since birth.
نویسندگان
چکیده
BACKGROUND Shah-Waardenburg syndrome is Waardenburg syndrome associated with Hirschsprung's disease. CASE CHARACTERISTICS A 10-day-old full-term male neonate of Waardenburg syndrome presented with constipation since birth along with features of small bowel obstruction. OBSERVATION Exploratory laparotomy revealed distended proximal jejunal and ileal loops along with microcolon; an ileostomy was performed. OUTCOME Postoperatively patient developed sepsis and died. Histopathology confirmed total colonic aganglionosis. MESSAGE Suspect familial Shah-Waardenburg syndrome in a neonate of Waardenburg syndrome presenting with constipation since birth or intestinal obstruction.
منابع مشابه
A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients
Waardenburg syndrome (WS) is a neurocristopathy with an autosomal dominant mode of inheritance, and considerable clinical and genetic heterogeneity. WS type II is the most common type of WS in many populations presenting with sensorineural hearing impairment, heterochromia iridis, hypoplastic blue eye, and pigmentary abnormalities of the hair and skin. To date, mutations of MITF, SOX10, and SNA...
متن کاملPerils of Total Colonic Aganglionosis Presenting in Neonatal Age
BACKGROUND The purpose of this study is to review the cases of total colonic aganglionosis seen in the span of ten years at a pediatric surgery unit of a tertiary care public hospital in New Delhi. METHODS Medical records of twelve patients with total colonic aganglionosis were retrieved. RESULTS Ten out of the twelve patients were males; seven were of the Muslim community. Average recorded...
متن کاملWaardenburg Syndrome in an Arab Family
By Laman Amin -ZaKI (Baghdad), The Journal of Laryngology and Otology, 1971.
متن کاملYoung Child with Down's Syndrome
An infant girl was diagnosed at birth as having Down's syndrome. Cytogenetic studies demonstrated a normal karyotype in the mother and trisomy 21 in the patient (Dr. E. Blank). In February 1963 the patient, aged 9 months, was admitted to the Children's Hospital, Sheffield, with acute laryngo-tracheo-bronchitis. At this time she was noted to have typical features of Down's syndrome (Fig. 1). Her...
متن کاملگزارش یک مورد سندروم واردنبرگنوع دو (گزارش مورد)
Waardenburg syndrome (WS) is a rare disease characterized by sensor neural deafness in association with pigmentary anomalies and defects of neural-crest-derived tissues. WS is caused by mutations in the microphthalmia-associated with transcription factor gene. This case is a 10 month old infant girl in which during a routine physical examination found that she has hetetrochromia and unilate...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Indian pediatrics
دوره 51 12 شماره
صفحات -
تاریخ انتشار 2014