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Apert syndrome: prenatal diagnosis challenge. [PDF]
BMJ Case Rep, 2019 Vieira C, Teixeira N, Cadilhe A, Reis I.
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Apert syndrome: Be aware of the 'dodgy' hip! [PDF]
BMJ Case Rep, 2018 Khan SA, Moores TS, Docker C.
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South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1972 openaire +1 more source
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Apert syndrome: A consensus on the management of Apert hands
Journal of Cranio-Maxillo-Facial Surgery, 2017Apert Syndrome is a congenital condition characterised by primary craniosynostosis, midfacial malformations and complex symmetrical malformations of the hands and feet. The hands demonstrate one of the most complex collections of congenital upper limb deformities, posing a significant challenge for the paediatric hand surgeon.
David A Pettitt, Paul Mcarthur
exaly +3 more sources
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
openaire +3 more sources
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
openaire +3 more sources
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
openaire +2 more sources
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
openaire +2 more sources