1 мая 2013 г. · Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the ... |
an extremely rare autosomal recessive [2] congenital disorder characterized by craniofacial malformations, obesity, syndactyly, and polydactyly. |
| Carpenter syndrome Болезнь или медицинское состояние |
Синдром Карпентера, также называемый акроцефалополисиндактилией типа II, является чрезвычайно редким аутосомно-рецессивным врожденным заболеванием, характеризующимся черепно-лицевыми пороками развития, ожирением, синдактилией и полидактилией. Википедия (Английский язык)
5 июл. 2022 г. · Carpenter syndrome is a rare genetic condition. The skull bones fuse too early, affecting brain development and facial features. |
Carpenter syndrome belongs to a group of rare genetic disorders known as “acrocephalopolysyndactyly” (ACPS) disorders. |
Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, ... |
In Carpenter syndrome, one or more of the sutures can fuse too early, causing the skull to be misshapen. |
A rare syndromic craniosynostosis with variable phenotypic expression characterized by craniosynostosis, intellectual disability, distinctive facies, ... |
Carpenter syndrome is an extremely rare condition affecting the skull and facial bones, as well as the bones of the hands and feet. |
Carpenter syndrome is a rare craniofacial genetic condition apparent at birth or shortly thereafter. Symptoms will vary widely among individuals from mild ... |
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