Pediatric bewer-way syndrome

Beckwith-Wiedemann syndrome is a rare congenital malformation, which is mainly characterized by umbilical bulge, giant tongue and giant body, and may be accompanied by other deformities and abnormalities, such as hypoglycemia, visceral hypertrophy, hypertrophy of the body, Small head, umbilical abnormalities, facial erythema, cryptorchidism, clitoral hypertrophy, cardiac malformation, giant kidney, giant ureter, giant eyeball, etc., have some relationship with some tumors. Pediatric-Weiy syndrome is autosomal dominant and may also be polygenic. Pediatric-Weiwer syndrome is also known as the umbilical cord, giant tongue, exomphalos-macroglossia-gigantism syndrome, EMG syndrome, Wiedemann type II syndrome, Wilm tumor and hepatomegaly syndrome, Beckwith syndrome, low newborn Neonatal hypoglycemia visceromegaly macroglossia microcephaly syndrome, etc.

The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.