Literature DB >> 3565473

Familial CHARGE syndrome: clinical report with autopsy findings.

L A Metlay, P S Smythe, M E Miller.   

Abstract

We report on a patient with CHARGE syndrome, as manifested by a coloboma of the optic nerve head, congenital heart defect (ASD, VSD, and parachute mitral valve), choanal atresia, severe growth retardation, genital hypoplasia, abnormal ears, cleft lip and palate, and pectus carinatum. His chromosomes were normal. He died at 19 months. His mother was short and had hearing impairment, choanal atresia, and a coloboma. We suggest that this represents evidence for dominant transmission of this disorder in this family. Other familial cases from the literature are reviewed.

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Year:  1987        PMID: 3565473     DOI: 10.1002/ajmg.1320260311

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  The CHARGE association.

Authors:  M G Bialer; W T Brown
Journal:  J Med Genet       Date:  1990-08       Impact factor: 6.318

2.  Who's in CHARGE? Multidisciplinary management of patients with CHARGE association.

Authors:  K D Blake; I M Russell-Eggitt; D W Morgan; J M Ratcliffe; R K Wyse
Journal:  Arch Dis Child       Date:  1990-02       Impact factor: 3.791

3.  Homeoboxes and field defects.

Authors:  J S Bamforth
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

4.  Congenital heart disease in CHARGE association.

Authors:  R K Wyse; S al-Mahdawi; J Burn; K Blake
Journal:  Pediatr Cardiol       Date:  1993-03       Impact factor: 1.655

5.  The eye in the CHARGE association.

Authors:  I M Russell-Eggitt; K D Blake; D S Taylor; R K Wyse
Journal:  Br J Ophthalmol       Date:  1990-07       Impact factor: 4.638

  5 in total

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