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Growth hormone deficiency in a case of cerebrofaciothoracic syndrome in one of two affected siblings

✍ Scribed by Kanaka-Gantenbein, Christina ;Fryssira, Helen ;Chrousos, George ;Mastorakos, George


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
26 KB
Volume
129A
Category
Article
ISSN
0148-7299

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Hypoplasia of the corpus callosum and gr
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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 histologic