Familial laryngomalacia in two siblings with syndromic features.

Abstract:

:We present two siblings with severe laryngomalacia requiring surgical intervention during the newborn period, microcephaly, developmental delay, cleft palate, preaxial polydactyly, dysplastic nails and conductive hearing loss (persistent after tympanostomy tube placement). In addition the girl has microopthalmia and the boy was born with a patent ductus arteriosus, mild pelviectasis, and hypospadias. This combination of multiple congenital anomalies has not been described previously and may represent a previously undescribed syndrome with autosomal inheritance.

authors

Chen JL,Messner AH,Chang KW

doi

10.1016/j.ijporl.2006.04.010

subject

Has Abstract

pub_date

2006-09-01 00:00:00

pages

1651-5

issue

9

eissn

0165-5876

issn

1872-8464

pii

S0165-5876(06)00140-6

journal_volume

70

pub_type

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