Cleidocranial dysplasia with growth hormone deficiency: a case report

• Ngā kaituhi matua: Nozomi Takaki (Author), Jun Mori (Author), Satoshi Matsuo (Author), Toshio Osamura (Author), Toshimi Michigami (Author)
• Hōputu: Pukapuka
• I whakaputaina: BMC, 2020-01-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

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...