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7p Deletion syndrome: An adult with mild manifestations

✍ Scribed by Grebe, Theresa A. ;Stevens, Mark A. ;Byrne-Essif, Karen ;Cassidy, Suzanne B.

Publisher: John Wiley and Sons
Year: 1992
Tongue: English
Weight: 436 KB
Volume: 44
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320440106

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✦ Synopsis

Deletion of 7p results in a wide spectrum of congenital abnormalities and minor facial and hand anomalies, often including craniosynostosis. We report on the oldest recognized patient with this disorder, a 24-year-old woman with an interstitial deletion from p15.3-p21.2 or p21.3. The manifestations in this patient are milder than those of previously described patients, and include borderline mental retardation, short stature, minor facial anomalies, and severa1 skeletal changes. The absence of craniosynostosis in this patient is noteworthy, given previous sug gestions that there is a specific locus for this finding in the 7p region. Twelve cases of 7p deletion, in which the missing segment overlaps that of the current case, are reviewed. This case delineates a broader spectrum for patients with 7p deletion syndrome.

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