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Acrocephalosyndactylia

Known as: Syndrome, Kurczynski Casperson, Acrocephalosyndactyly, Kurczynski Casperson Syndrome 
A genetic disorder characterized by craniosynostosis and fusion of the fingers and toes.
National Institutes of Health

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ACROCEPHALOPOLYSYNDACTYLY TYPE IVApert syndromeApert-Crouzon DiseaseCardiocranial syndrome
AcrocephalopolysyndactylyAcrocephalopolysyndactyly type 2Congenital musculoskeletal anomaliesCraniofacial Dysostosis

Papers overview

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2015
2015
Características bucais e craniofaciais da síndrome de Apert: relato de caso
A sindrome de Apert, tambem conhecida como acrocefalossindactilia e uma rara condicao genetica caracterizada pela fusao prematura… 
2009
2009
Apert syndrome
A guide to diagnosis and treatment 
2002
2002
Surgical Correction of the Apert Craniofacial Deformities
Apert first utilized the term acrocephalosyndactyly in 1906 to describe a foreshortened, tower-shaped cranial malformation… 
1994
1994
Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from…
Craniosynostosis (premature fusion of the skull sutures) occurs as a clinically heterogeneous group of disorders, frequently… 
1985
1985
[Acrocephalosyndactylia--Vogt syndrome].
A genetically remarkable case of the Vogt syndrome (combination of the Apert and Crouzon syndromes) associated with a dysraphia… 
1983
1983
[Acrocephaly, cranial asymmetry, brachydactyly, syndactyly, progressive senile dementia--a new type of acrocephalosyndactyly?].
Clinicogenetic assessment of a family whose six members proved to be carriers of an identical pathological trait allowed the… 
1971
1971
Apert's acrocephalosyndactyly in mother and daughter: cleft palate in the mother.
1971
1971
Apert's acrocephalosyndactyly in mother and daughter: cleft palate in the mother.
1970
1970
Acrocephalosyndactylia associated with a chromosomal translocation. 46,XX, t (2p-; Cq+).
An infant with typical acrocephalosyndactylia was found to have a consistently present deletion-translocation of the short arms… 
1969
1969
[Ocular manifestations during acrocephalosyndactyly (Apert's disease) (with presentation of 2 more cases)].