Results 101 to 110 of about 665 (159)

3D Printing Today, AI Tomorrow: Rethinking Apert Syndrome Surgery in Low-Resource Settings. [PDF]

Healthcare (Basel)
Bajwa M, Pasha M, Bajwa Z.
europepmc   +1 more source

Idiopathic Syringomyelia: Diagnostic Value of Cranial Morphometric Parameters. [PDF]

Brain Sci
Özkal B, Özçelik H.
europepmc   +1 more source

Genetic Variants in DVL3 are Associated With Root Maldevelopment, Tooth Agenesis, Mesiodens, and Oral Exostoses. [PDF]

Int Dent J
Kantaputra P, Bunpiem N, Guven Y, Tripuwabhrut K, Kalayci T, Imren E, Sengtae N, Pianmee C, Pruksametanan A, Tongsima S, Ngamphiw C, Kawasaki K, Ohazama A, Cairns JRK.   +13 more
europepmc   +1 more source

Inferior Outcomes of Posterior Correction and Fusion Surgery for Adults With Residual Lenke Type 5 Adolescent Idiopathic Scoliosis: A Comparative Study With Adolescents. [PDF]

Global Spine J
Shibata R, Suzuki S, Takeda K, Iga T, Okubo T, Ozaki M, Tsuji O, Nagoshi N, Matsumoto M, Nakamura M, Watanabe K.   +10 more
europepmc   +1 more source

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Acrocephalosyndactyly (Apert's Syndrome)

JAMA Ophthalmology, 1967
A 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.
S Gärtner
exaly   +3 more sources

Otologic Manifestations of Acrocephalosyndactyly

Archives of Otolaryngology, 1972
Four patients with Apert's acrocephalosyndactyly were found to have congenital maximum conductive hearing losses. A congenitally fixed stapes footplate and perilymph gusher, suggesting abnormally patent cochlear aqueduct, was found in the ear of one patient, whose mother also had the syndrome. In another young adult Negro patient with stable, long-term
William G Hemenway, Lavonne Bergstrom, L Bergström   +2 more
exaly   +3 more sources

On the Classification of the Acrocephalosyndactyly Syndromes

Clinical Genetics, 1977
This report describes a family in which two different types of acrocephalosyndactyly (ACS) were clinically identified. The proband presented with the classic stigmata of Pfeiffer syndrome, while her cousin was considered to be a typical case of Apert syndrome.
David Bixler, V Escobar
exaly   +3 more sources