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Review
. 1989 Apr;35(4):293-8.
doi: 10.1111/j.1399-0004.1989.tb02947.x.

Trisomy 9q3 syndrome: a case report and review of the literature

K Naritomi  1 , Y Izumikawa, Y Goya, M Gushiken, N Shiroma, K Hirayama
Affiliations
Review

Trisomy 9q3 syndrome: a case report and review of the literature

K Naritomi et al. Clin Genet. 1989 Apr.

Abstract

A girl with partial trisomy 9q is reported. She was characterized by dolichomorphism, abnormalities of the digits, a cardiac defect and craniofacial dysmorphism. A high-resolution analysis revealed the karyotype to be: 46,XX,-3,+ der(3)t(3;9)(q29;q13) de novo. A phenotype-karyotype correlation study in 22 cases of partial trisomies 9q supported the delineation of a trisomy 9q3 syndrome. The smallest region of overlap was confined to 9q32.

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