14 сент. 2022 г. · Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial appearance, eye abnormalities, hearing loss, ... |
Stickler syndrome (hereditary progressive arthro-ophthalmodystrophy) is a group of rare genetic disorders affecting connective tissue, specifically collagen. |
Stickler syndrome is characterized by the following clinical features: vitreoretinal degeneration, myopia, cataracts, retinal holes and detachments, ... |
Disease definition. A rare group of genetic connective tissue disorders characterized by ophthalmic, auditory, orofacial and articular manifestations. |
| Синдром Стиклера Заболевание |
Синдром Стиклера — группа наследственных коллагенопатий, впервые описанная Г. Стиклером в 1965. Другое название — наследственная артроофтальмопатия. Заболевание характеризуется измениями лица, поражением глаз, потерей слуха и патологией суставов. Википедия
МКБ-10 : Q87.8
МКБ-9 : 759.89
62938-3/asset/7c28d774-7491-4b8a-8336-f45c0bc93750/main.assets/gr1_lrg.jpg)
30 сент. 2024 г. · Stickler syndrome is a genetic disorder that causes joint, hearing, and vision problems. It affects collagen, the connective tissue of the ... |
| Novbeti > |
| Axtarisha Qayit Anarim.Az Anarim.Az Sayt Rehberliyi ile Elaqe Saytdan Istifade Qaydalari Anarim.Az 2004-2023 |