Carpenter syndrome is an autosomal recessive disease which means both parents must have the faulty genes in order to pass the disease onto their children. Even if both parents possess the …

What is Carpenter syndrome? Carpenter syndrome is a rare inherited genetic disorder. Its main symptom is craniosynostosis, a congenital defect (meaning a person is born with it) that …

Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other developmental problems. …

Carpenter syndrome can be caused by genetic changes in the RAB23 or MEGF8 gene and is inherited in an autosomal recessive manner. Carpenter syndrome is a condition characterized …

Carpenter syndrome is also known as ACPS type II. Carpenter syndrome is typically evident at or shortly after birth. Due to craniosynostosis, the top of the head may appear unusually conical …

Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other developmental …

Carpenter syndrome is the rarest, with only occasional patients seen. There are 3 common features in all of these syndromes: craniosynostosis (skull base abnormalities, with early …

Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other developmental problems. …

Carpenter syndrome is an extremely rare condition affecting the skull and facial bones, as well as the bones of the hands and feet. It is estimated to occur in approximately 1 in 1,000,000 births. …

Information and support for people affected by the autosomal recessive genetic disorder, Carpenter Syndrome.