A DIDMOAD syndrome family with juvenile glaucoma and myopia findings
Acta Ophthalmologica Scandinavica, cilt.78, sa.4, ss.480-482, 2000 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 78 Sayı: 4
- Basım Tarihi: 2000
- Doi Numarası: 10.1034/j.1600-0420.2000.078004480.x
- Dergi Adı: Acta Ophthalmologica Scandinavica
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.480-482
- Anahtar Kelimeler: DIDMOAD syndrome, diabetes mellitus, diabetes insipidus, optic atrophy, deafness, juvenile glaucoma, myopia, posterior polar cataract
- Sağlık Bilimleri Üniversitesi Adresli: Hayır
Özet
We present here two DIDMOAD syndrome cases (Diabetes Mellitus, Diabetes Insipidus, Optic Atrophy, Deafness) in a Turkish family. In the examination of the propositus who had consanguineous parents, diabetes mellitus, diabetes insipidus, optic atrophy, and deafness were observed in addition to myopia, juvenile glaucoma, posterior polar cataract, and dilatation of the urinary tract. Diabetes mellitus, diabetes inspidus, optic atrophy, deafness, myopia, and ventricular septal defect were observed in his elder brother. Juvenile onset diabetes mellitus, congenital glaucoma, deafness, and heart disease were the other remarkable findings observed in relatives to this family. Juvenile glaucoma, posterior polar cataract observed in our propositus, and myopia in both our DIDMOAD syndrome cases are the first ophthalmic manifestations described in the DIDMOAD syndrome.