While there are some significant differences, a good point of reference is it's similarity to Pfeiffer and Apert Syndromes. 1A).Syndactyly is a characteristic feature of AS that permits distinction from the other FGFR2-related syndromes, and shows a complex fusion leading to 'mitten hand' deformity in both hands and feet. However, some individuals with this condition have normal intelligence. At a clinical level, Apert syndrome is characterized by the presence or development of a pointed or elongated skull, sunken facial […] ACPS disorders are characterized by issues with the skull, fingers, and toes. This report presents five cases of Apert's syndrome with features of acrocephaly, characteristic face and complete syndactyly of the hand and foot wit… Carpenter syndrome is the … There is no blood test or X-ray needed; Carpenter syndrome is typically diagnosed solely through a physical examination. Carpenter syndrome is an extremely rare congenital (present at birth) disorder that causes abnormal growth of a baby’s skull, fingers, and toes. It is a form of acrocephalopolysyndactyly (ACPS) which is a group of genetic disorders that are rare and they include Apert syndrome. The signs and symptoms of Carpenter syndrome can vary greatly, even within … This early fusion prevents the skull from growing normally and affects the shape of the head and face. Know all about the causes, symptoms, diagnosis and treatment for Apert Syndrome. Apert syndrome. He described two sisters and a brother with acrocephaly (cone shaped heads), peculiar facies, brachydactyly (abnormally short fingers), syndactyly (webbing) of the fingers and toes, and polydactyly (extra digits). Babies born with Carpenter syndrome have skull bones that fuse too early and webbed, unusually short, or extra fingers and toes. Carpenter's Syndrome is a genetic birth defect syndrome that involves the toes, fingers, skull and sometimes even the heart. This can occur in babies with no family history of the disorder, or they can inherit it from a parent. Carpenter syndrome is a rare autosomal recessive disorder that belongs to a group of rare craniosynostosis syndromes (Bull Soc Med Paris 1906;23:1310). Babies born with Carpenter syndrome have skull bones that fuse too early and webbed, unusually short, or extra fingers and toes. Carpenter syndrome is a rare autosomal recessive disorder that belongs to a group of rare craniosynostosis syndromes (Bull Soc Med Paris 1906;23:1310). It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible.Disturbances in the development of the branchial arches in fetal development create lasting and widespread effects.