Craniosynostosis, Philadelphia type | |
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Autosomal dominant inheritance |
Craniosynostosis, Philadelphia type is a rare autosomal dominant syndrome characterized by sagittal craniosynostosis ( scaphocephaly) and soft tissue syndactyly of the hands and feet. This condition is considered a form of acrocephalosyndactyly. [1] [2] [3]
Features of this condition include: [1] [3]
Facial features in this condition are usually normal.
In 1996, a distinct form of acrocephalosyndactyly was reported in five generations of a single family. Over these five generations, an autosomal dominant pattern of sagittal craniosynostosis and soft tissue syndactyly was noted. The syndactyly was mitten-like and resembled Apert syndrome but was excluded as being caused by Apert syndrome due to the lack of bony involvement. [2]
This condition is caused by duplications in chromosome 2 near-identical to those responsible for syndactyly type 1 (Chromosome 2q35 Duplication Syndrome). [2]
Craniosynostosis, Philadelphia type | |
---|---|
![]() | |
Autosomal dominant inheritance |
Craniosynostosis, Philadelphia type is a rare autosomal dominant syndrome characterized by sagittal craniosynostosis ( scaphocephaly) and soft tissue syndactyly of the hands and feet. This condition is considered a form of acrocephalosyndactyly. [1] [2] [3]
Features of this condition include: [1] [3]
Facial features in this condition are usually normal.
In 1996, a distinct form of acrocephalosyndactyly was reported in five generations of a single family. Over these five generations, an autosomal dominant pattern of sagittal craniosynostosis and soft tissue syndactyly was noted. The syndactyly was mitten-like and resembled Apert syndrome but was excluded as being caused by Apert syndrome due to the lack of bony involvement. [2]
This condition is caused by duplications in chromosome 2 near-identical to those responsible for syndactyly type 1 (Chromosome 2q35 Duplication Syndrome). [2]