Saethre-Chotzen Syndrome
This malformation syndrome is named after two psychiatrists who independently described it.
Saethre-Chotzen syndrome
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Saethre-Chotzen syndrome --
type III acrocephalosyndactyly
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Can Saethre-Chotzen syndrome be inherited?
This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.
Saethre-Chotzen syndrome belongs to a group of rare genetic disorders known as "acrocephalosyndactyly" disorders.
Related Articles The frequency of palatal anomalies in Saethre-Chotzen syndrome.… more…
Sudden Death in a Child With Carpenter… ...
Apert syndrome (Acrocephalosyndactyly type I) can be distinguished from two related conditions, acrocephalopolysyndactyly type II (Carpenter syndrome) and acrocephalosyndactyly type III (Saethre-Chotzen syndrome).
Carpenter syndrome (kleeblattschadel, cloverleaf skull deformity)
Crouzon disease (craniofacial dysostosis)
Saethre-Chotzen syndrome
Pfeiffer syndrome ...
brain's growth is inhibited and your child's head develops into an abnormal shape. Other conditions often associated with craniosynostosis include Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, Carpenter syndrome and Saethre-Chotzen syndrome.
Phonocardiographies, Phosphatases, Protein, Phylloquinone Reductase, Pivoxil, Amdinocillin, Polygenic Characters, Pregnanolone, (3alpha,5beta)-isomer, Presomen, Programmed Instruction, Blockaders, H1 Receptor, S6 Kinase, Saethre-Chotzen Syndrome, ...
 See also: Autosomal dominant, Craniosynostosis, Fusion, Syndactyly, Apert syndrome
  
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