Results 141 to 150 of about 809 (163)
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Acrocephalosyndactyly with report of a case

The British Journal of Radiology, 1953
A case of Acrocephalosyndactyly, as first described by Apert, is reported. Reference is made to the high degree of function developed by the patient in grossly deformed hands and feet. There is no evidence that this case is familial and a review and discussion of some of the literature indicates that the condition belongs to the group of skull ...
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Acrocephalosyndactyly

2011
The Radswiki, Arlene Campos, Henry Knipe
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[Acrocephalosyndactyly (ACS) (author's transl)].

Anales espanoles de pediatria, 1976
13 cases of ACS are presented: seven of them were identified as Apert's syndrome; two as Chotzen's syndrome; three as Carpenter's syndrome, and one as Pfeiffer's syndrome. These disorders have no known ethiology. However, it is necessary to look for diabetic antecedents and dermatogliphus alterations, both in the patient and the parents.
A V, Fajardo Carmona   +1 more
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Autosomal recessive acrocephalosyndactyly revisited

American Journal of Medical Genetics, 1980
J G, Hall   +3 more
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Acrocephalosyndactyly

2009
Hubert Scharnagl   +199 more
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Acrocephalosyndactyly

Chulalongkorn Medical Journal, 1967
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[Acrocephalosyndactyly I (Apert syndrome)].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2001
A fourteen years old girl showed the classic signs of acrocephalosyndactyly I: dysostosis craniofacialis with hypertelorism, exophthalmus, strabism, amblyopia and cleft palate as well as syndactyly of the fingers and toes. The feet showed on both side a 6 cm long horny band.
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[Acrocephalosyndactyly].

Neurocirugia, 2002
H, CARNICA, G, MAYERSTEIN, R, POBLETE
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