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DOI 10.1097/00125817-200101000-00009

Медицинская библиотека · Genetics in medicine : official journal of the American College of Medical Genetics · 2001

Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion.

Gerdes M, Solot C, Wang P P, McDonald-McGinn D M, Zackai E H

СтатьяПоддержка службы здравоохранения СШАПеревод пока не подготовлен

Аннотация

PURPOSE: The purpose of this study is to review the neurodevelopmental outcome of infants and preschoolers with a 22q11.2 microdeletion and to discuss the our clinical observations of clinical implications for educational and therapeutic interventions.

METHODS

One hundred twelve children (4 to 70 mos) with the 22q11.2 deletion were assessed using standardized tests (Bayley Scales of Infant Development-II, Preschool Language Scales, Wechsler Preschool and Primary Scales of Intelligence-Revised).

RESULTS

Fifty-four percent of the children were significantly delayed, 24% had mild delay, 22% had average cognitive development, and 80% were below average in language development. Delays are not explained by cardiac defects or palatal defects.

CONCLUSION

Developmental delays, mild hypotonia, language and speech delays, and feeding disorders are common, and this finding indicates the need for early intervention services beginning in infancy for children with the 22q11.2 deletion.

Для цитирования: Gerdes M, Solot C, Wang P P, McDonald-McGinn D M, Zackai E H. Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion.. Genetics in medicine : official journal of the American College of Medical Genetics. 2001. DOI: 10.1097/00125817-200101000-00009.

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