Ophthalmic features of CHARGE syndrome with CHD7 mutations

Sachiko Nishina, Rika Kosaki, Tatsuhiko Yagihashi, Noriyuki Azuma, Nobuhiko Okamoto, Yoshikazu Hatsukawa, Kenji Kurosawa, Takahiro Yamane, Seiji Mizuno, Kinichi Tsuzuki, Kenjiro Kosaki

研究成果: Article査読

12 被引用数 (Scopus)


Coloboma and various ocular abnormalities have been described in CHARGE syndrome, although the severity of visual impairment varies from case to case. We conducted a multicenter study to clarify the ophthalmic features of patients with molecularly confirmed CHARGE syndrome. Thirty-eight eyes in 19 patients with CHARGE syndrome and confirmed CHD7 mutations treated at four centers were retrospectively studied. Colobomata affected the posterior segment of 35 eyes in 18 patients. Both retinochoroidal and optic disk colobomata were bilaterally observed in 15 patients and unilaterally observed in 3 patients. The coloboma involved the macula totally or partially in 21 eyes of 13 patients. We confirmed that bilateral large retinochoroidal colobomata represents a typical ophthalmic feature of CHARGE syndrome in patients with confirmed CHD7 mutations; however, even eyes with large colobomata can form maculas. The anatomical severity of the eye defect was graded according to the presence of colobomata, macula defect, and microphthalmos. A comparison of the severity in one eye with that in the other eye revealed a low-to-moderate degree of agreement between the two eyes, reflecting the general facial asymmetry of patients with CHARGE syndrome. The location of protein truncation and the anatomical severity of the eyes were significantly correlated. We suggested that the early diagnosis of retinal morphology and function may be beneficial to patients, since such attention may determine whether treatment for amblyopia, such as optical correction and patching, will be effective in facilitating the visual potential or whether care for poor vision will be needed.

ジャーナルAmerican Journal of Medical Genetics, Part A
158 A
出版ステータスPublished - 2012 3

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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