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Indian pediatrics, 1977 Some of the next articles are maybe not open access.
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International Journal of Dermatology, 2006
AbstractApert syndrome or acrocephalosyndactyly is a rare autosomal dominant malformation syndrome characterized by craniosynostosis, symmetric severe syndactyly, and a variety of abnormalities of the skin, skeleton, brain, and visceral organs. A case of Apert syndrome and the clinical and specific cutaneous manifestations of this condition are ...
Anatoli, Freiman +2 more
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AbstractApert syndrome or acrocephalosyndactyly is a rare autosomal dominant malformation syndrome characterized by craniosynostosis, symmetric severe syndactyly, and a variety of abnormalities of the skin, skeleton, brain, and visceral organs. A case of Apert syndrome and the clinical and specific cutaneous manifestations of this condition are ...
Anatoli, Freiman +2 more
openaire +3 more sources
Child's Nervous System, 1993
This paper discusses 33 cases of Apert's syndrome which were treated in the Australian Craniofacial unit at the adelaide Children's Hospital. The main features were discussed. We found that mild ventricular dilatation is common in Apert's syndrome but without associated raised intracranial pressure.
A, Hanieh, D J, David
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This paper discusses 33 cases of Apert's syndrome which were treated in the Australian Craniofacial unit at the adelaide Children's Hospital. The main features were discussed. We found that mild ventricular dilatation is common in Apert's syndrome but without associated raised intracranial pressure.
A, Hanieh, D J, David
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Postgraduate Medicine, 1969
Apert's syndrome is a rare condition characterized by a tetrad of features: acrocephaly, facial deformities, ocular proptosis with visual defect, and syndactyly. The patient in the case described is a 13 year old girl without a family history of similar anomalies.
J A, Hall, C V, Lewis
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Apert's syndrome is a rare condition characterized by a tetrad of features: acrocephaly, facial deformities, ocular proptosis with visual defect, and syndactyly. The patient in the case described is a 13 year old girl without a family history of similar anomalies.
J A, Hall, C V, Lewis
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Acrocephalosyndactyly (Apert's Syndrome)
Archives of Ophthalmology, 1967A case of acrocephalosyndactyly in a 63-year-old woman is reported. The intelligence, sex, and racial distribution, hereditary tendency, and chromosomal analysis of acrocephalosyndactyly is discussed. Ocular complications of this syndrome were noted to be mainly optic atrophy, exophthalmos, and strabismus.
M, Seelenfreund, S, Gartner
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International Journal of Nursing Education and Research, 2021
Apert syndrome is another genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting skull and facial deformities and syndactyly. The syndrome was first described in 1906 by French physician Eugene Apert when he described nine people with similar facial and extremity characteristics. In 1906, Eugène
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Apert syndrome is another genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting skull and facial deformities and syndactyly. The syndrome was first described in 1906 by French physician Eugene Apert when he described nine people with similar facial and extremity characteristics. In 1906, Eugène
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Cutis, 1980
We report herein a case of Apert's syndrome, which is characterized clinically by cranial, facial, and limb malformations. Acne vulgaris of the upper extremities constitutes the dermatologic hallmark of this rarely reported disorder.
P Z, McNaughton, O G, Rodman
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We report herein a case of Apert's syndrome, which is characterized clinically by cranial, facial, and limb malformations. Acne vulgaris of the upper extremities constitutes the dermatologic hallmark of this rarely reported disorder.
P Z, McNaughton, O G, Rodman
openaire +1 more source