Literature DB >> 9714686

The CHARGE association in a newborn infant.

M Akisü1, F Ozkinay, R Ozyürek, A Küçüktaş, N Kültürsay.   

Abstract

CHARGE association is the nonrandom association of congenital anomalies, including choanal atresia, coloboma, heart defects, retardation of growth and development, genital hypoplasia and ear abnormalities. We report a male newborn infant with CHARGE association. Other congenital abnormalities include micrognathia, high-arched palate, facial asymmetry, broad nasal bridge, hypertelorism, asymmetric eye size, and left microphthalmia. On radiologic examination, hemivertebrae were detected on the thoracal vertebrae. Although both autosomal and recessive transmission have been reported, most cases of CHARGE association have been sporadic (karyotype analysis is generally reported to be normal as in our patient). Transmission and recurrence risk of this association are not known. The presence of choanal atresia and/or coloboma must alert the clinician to search for other abnormalities for diagnosis of CHARGE association.

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Year:  1998        PMID: 9714686

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  2 in total

1.  The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.

Authors:  Ethan D Sperry; Elizabeth A Hurd; Mark A Durham; Elyse N Reamer; Adam B Stein; Donna M Martin
Journal:  Dev Dyn       Date:  2014-07-10       Impact factor: 3.780

2.  Role of Chd7 in zebrafish: a model for CHARGE syndrome.

Authors:  Shunmoogum A Patten; Nicole L Jacobs-McDaniels; Charlotte Zaouter; Pierre Drapeau; R Craig Albertson; Florina Moldovan
Journal:  PLoS One       Date:  2012-02-20       Impact factor: 3.240

  2 in total

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