treacher collins syndrome - Axtarish в Google
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Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. The degree to which a person is ...
Синдром Тричера Коллинза Заболевание
Синдром Тричера Коллинза — аутосомно-доминантное заболевание, характеризующееся черепно-лицевой деформацией. Описан английским офтальмологом Эдвардом Тричером Коллинзом в 1900 году. Синдром Тричера Коллинза встречается у 1 из 50 000 младенцев. Википедия
МКБ-10 : Q75.4
МКБ-11 : LD2F.16
МКБ-9 : 756.0
9 дек. 2022 г. · Treacher Collins syndrome is a condition that affects the development of bones and other tissues of the face. Explore symptoms, inheritance ...
Treacher Collins syndrome is a rare inherited group of conditions that affects the growth of a child's skull and facial bones.
1 нояб. 2023 г. · Treacher Collins syndrome (TCS) is a rare genetic disorder characterized by distinctive features of the head and face. Craniofacial differences ...
Treacher-Collins syndrome (also known as mandibulofacial dysostosis) is a congenital (present at birth) condition affecting the bones and tissues in the ...
Treacher Collins syndrome is a genetic disorder that affects growth and development of the head, causing facial defects and hearing loss.
Treacher Collins syndrome is a rare, genetic condition affecting the way the face develops — especially the cheekbones, jaws, ears and eyelids.
Treacher Collins syndrome is a genetic disorder resulting in congenital craniofacial malformation. Patients typically present with downslanting palpebral ...
Treacher Collins syndrome (TCS) refers to a group of facial features that some babies are born with. TCS causes distinctive abnormalities of the head and ...
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