Cleidocranial dysplasia with growth hormone deficiency: a case report

Abstract Background Cleidocranial dysplasia (CCD) is a rare skeletal disorder with autosomal dominant inheritance that is characterized by hypoplastic clavicles, delayed closure of the cranial sutures, dental abnormalities, and short stature, among other features. The responsible gene for CCD is RUN...

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Bibliographic Details
Main Authors: Nozomi Takaki (Author), Jun Mori (Author), Satoshi Matsuo (Author), Toshio Osamura (Author), Toshimi Michigami (Author)
Format: Book
Published: BMC, 2020-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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