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CHARGE association in Sweden: malformations and functional deficits.
- Source :
-
American journal of medical genetics. Part A [Am J Med Genet A] 2005 Mar 15; Vol. 133A (3), pp. 331-9. - Publication Year :
- 2005
-
Abstract
- CHARGE association (CA) consists of a non-random association of ocular coloboma (C), heart anomaly (H), atresia of choanae (A), retarded growth and/or development (R), genital hypoplasia (G), and ear anomalies and/or hearing impairment (E). A prospective multidisciplinary study of 31 Swedish patients with CA was undertaken in order to describe the associated malformations and functional deficits, find possible etiological factors and identify critical time periods for the maldevelopment. The clinical files were analyzed, the mothers answered a questionnaire on history of prenatal events, and a clinical evaluation of systemic findings, vision, hearing, balance, speech, oral and swallowing function, and neuro-psychiatric function, especially autism, was performed. The most frequent physical abnormalities affected ears (90%), eyes (90%), brain (61%), heart (52%), retarded growth (48%), genitals (38%), choanae (35%), and facial nerve (32%). Sixty-one percent of the patients were visually impaired or blind, and 74% had hearing loss or deafness. Problems in balance, speech, and eating were common. Forty percent of the patients had autism/atypical autism, and 82% had developmental delay. Three children were born following assisted fertilization and two mothers had diabetes. The mothers reported infections, bleedings, and drug use during pregnancy. Analysis of possible critical time periods suggested that most malformations were produced early in pregnancy, mainly during post conceptual weeks 4, 5, and 6. A multidisciplinary approach is essential in the assessment and management of CA.<br /> (Copyright (c) 2005 Wiley-Liss, Inc.)
- Subjects :
- Abnormalities, Multiple etiology
Abnormalities, Multiple physiopathology
Adolescent
Adult
Autistic Disorder pathology
Autistic Disorder physiopathology
Child
Child, Preschool
Deafness pathology
Ear abnormalities
Female
Genitalia abnormalities
Growth Disorders pathology
Humans
Infant
Infant, Newborn
Male
Maternal Age
Paternal Age
Risk Factors
Sweden
Syndrome
Abnormalities, Multiple pathology
Choanal Atresia pathology
Coloboma pathology
Heart Defects, Congenital pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1552-4825
- Volume :
- 133A
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics. Part A
- Publication Type :
- Academic Journal
- Accession number :
- 15633180
- Full Text :
- https://doi.org/10.1002/ajmg.a.30563