apert syndrome - Axtarish в Google
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Синдром Аперта Заболевание
Синдром Апе́ра — врожденная аномалия развития черепа, которая сочетается с отклонением развития кистей рук. Раннее закрытие венечного и стреловидного швов способствует деформации черепа, что приводит к внутричерепной гипертензии. Синдром Аперта... Википедия
МКБ-10 : Q87.0
МКБ-11 : LD24.G2
МКБ-9 : 755.55
Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones. It is characterized by ...
1 авг. 2019 г. · Apert syndrome is a genetic disorder characterized by skeletal abnormalities. Explore symptoms, inheritance, genetics of this condition.
Apert syndrome is a rare genetic condition that causes a baby's skull, face, feet and hands to form atypically when the skull joints close too soon.
Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet.
Apert syndrome is a genetic disease affecting the shape of the head and face that also includes anomalies of the limbs and hands. What is Apert Syndrome? · Treatment
30 июл. 2019 г. · Apert syndrome is a rare genetic condition that is apparent at birth. People with Apert syndrome can have distinctive malformations of the skull ...
Apert syndrome is a genetic condition, caused by a mutation (change) on a specific gene. Research has identified the affected gene as the Fibroblast Growth ...
6 дек. 2022 г. · AxtarishMD describes Apert syndrome, a genetic disorder that can cause abnormalities in the formation of the head and other parts of the body.
16 авг. 2022 г. · Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and severe symmetrical ...
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