Endocrinological Characteristics of 25 Japanese Patients with CHARGE Syndrome

نویسندگان

  • Yasuko Shoji
  • Shinobu Ida
  • Yuri Etani
  • Hiroyuki Yamada
  • Futoshi Kayatani
  • Yasuhiro Suzuki
  • Kenjiro Kosaki
  • Nobuhiko Okamoto
چکیده

CHARGE syndrome is a congenital disorder caused by mutation of the chromodomain helicase DNA binding protein 7 (CHD7) gene and is characterized by multiple anomalies including ocular coloboma, heart defects, choanal atresia, retarded growth and development, genital and/or urological abnormalities, ear anomalies, and hearing loss. In the present study, 76% of subjects had some type of endocrine disorder: short stature (72%), hypogonadotropic hypogonadism (60%), hypothyroidism (16%), and combined hypopituitarism (8%). A mutation in CHD7 was found in 80% of subjects. Here, we report the phenotypic spectrum of 25 Japanese patients with CHARGE syndrome, including their endocrinological features.

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عنوان ژورنال:

دوره 23  شماره 

صفحات  -

تاریخ انتشار 2014