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Hypoplasia of the corpus callosum and growth hormone deficiency in the XXXXY syndrome

✍ Scribed by Haeusler, Gabriele ;Frisch, H. ;Guchev, Z. ;Hadziselimovic, F. ;Neuhold, A. ;Vormittag, W.

Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
361 KB
Volume
44
Category
Article
ISSN
0148-7299

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✦ Synopsis

A 3-year-old Libyan boy with the XXXXY syndrome is described. MRI examination of the brain showed hypoplasia of the corpus callosum. He had growth retardation and endocrine studies demonstrated growth hormone (GH) deficiency. Derrnatoglyphic pattern was different from previous reports. At histological examination of the undescended testes, Leydig cells were seen although they are usually not found in this variant of the Klinefelter syndrome.

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