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Carpenter syndrome
- Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other ...
- ... the RAB23 gene have been found to cause Carpenter syndrome, a condition characterized by irregular skull formation, finger ... mutation that is frequently seen in individuals with Carpenter syndrome who are of northern European ancestry replaces the ...
- ... the MEGF8 gene have been found to cause Carpenter syndrome, a condition characterized by irregular skull formation, finger ... It is unclear how MEGF8 gene mutations cause Carpenter syndrome. The mutations likely interfere with normal patterning of ...
- Alpha thalassemia X-linked intellectual disability syndrome is an inherited disorder that affects many parts of the body. This condition occurs almost exclusively ...
- ... Hereditary syndactyly Very rare causes include: Apert syndrome Carpenter syndrome Cornelia de Lange syndrome Pfeiffer syndrome Smith-Lemli- ...
- ... after birth Congenital craniosynostosis Crouzon syndrome Apert syndrome Carpenter syndrome Pfeiffer syndrome
- ... features of Apert syndrome. These similar syndromes include: Carpenter syndrome (kleeblattschadel, cloverleaf skull deformity) Crouzon disease (craniofacial dysostosis) ...
- Craniofacial Abnormalities (National Library of Medicine)Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
- Causes may include: Asphyxiating thoracic dystrophy Carpenter syndrome Ellis-van Creveld syndrome (chondroectodermal dysplasia) Familial polydactyly Laurence-Moon-Biedl syndrome Rubinstein-Taybi syndrome Smith-Lemli-Opitz syndrome Trisomy 13
- ... disorders commonly linked to craniosynostosis include Crouzon, Apert, Carpenter, Saethre-Chotzen, and Pfeiffer syndromes. However, most children with craniosynostosis are otherwise healthy ...
