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Growth hormone treatment in a child with Williams-Beuren syndrome: a case report

✍ Scribed by G. M. C. Kuijpers; M. De Vroede; H. E. Knol; M. Jansen


Publisher
Springer
Year
1999
Tongue
English
Weight
110 KB
Volume
158
Category
Article
ISSN
0340-6997

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## Abstract We report a 19‐month‐old boy with microcephaly, growth and developmental delay, facial dysmorphisms, and simplified gyral pattern. Magnetic resonance imaging (MRI) examination demonstrated microcephaly with simplified gyral pattern or oligogyric microcephaly. The facial phenotype was in