stickler syndrome - Axtarish в Google
14 сент. 2022 г. · Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial appearance, eye abnormalities, hearing loss, ...
Stickler syndrome is a genetic condition that affects connective tissues in your face and joints, leading to problems with vision, hearing and movement.
7 сент. 2023 г. · Stickler syndrome is a connective tissue disorder that can include ocular findings of myopia, cataract, and retinal detachment; hearing loss ...
Stickler syndrome is a relatively common congenital (present at birth) condition that affects the formation of a connective tissue called collagen.
13 июн. 2024 г. · Stickler syndrome is a systemic connective tissue disorder characterized by defective collagen production.
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
Disease definition. A rare group of genetic connective tissue disorders characterized by ophthalmic, auditory, orofacial and articular manifestations.
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, ...
Stickler syndrome is a group of genetic conditions that affects connective tissue, specifically collagen. The condition is characterized by facial ...
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 ...
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