Results 111 to 120 of about 5,186 (188)
Pathogenic de novo mutations increase with fathers' age and could be amplified through competition between genetically distinct subpopulations of spermatogonial stem cells (SSCs).
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Apert Syndrome - caveats of squint management. [PDF]
Rom J Ophthalmol, 2023 Khurana R, Singh A, Kochhar D, Sundar S.
europepmc +1 more source
Identification of the molecular basis of the lacrimo-auriculo-dento-digital (LADD) syndrome [PDF]
, 2008 Lacrimo-auriculo-dento-digital (LADD) syndrome, also known as Levy-Hollister syndrome, is a rare autosomal dominant developmental disorder, mainly characterized by abnormalities of the lacrimal system and salivary glands, ears and hearing, teeth and ...
Rohmann, Edyta
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Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers. [PDF]
Cureus, 2023 Kumari K +10 more
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Brain and ventricular volume in patients with syndromic and complex craniosynostosis [PDF]
, 2011 T. de Jong +4 more
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Anesthesia and Airway Management in Two Cases of Apert Syndrome: Case Reports
Eurasian Journal of Medicine, 2019 Apert syndrome is a type of acrocephalosyndactilia that consists of craniofacial synostosis, midface hypoplasia and syndactyly, with an autosomal dominant inheritance pattern.
Canan Atalay +3 more
doaj
Outcome of Bilateral Hand Reconstruction in a Child Presenting Late With Apert Syndrome: A Case Report and Literature Review. [PDF]
Cureus, 2023 Lim B, Shalan M.
europepmc +1 more source
Apert Syndrome: Dental management considerations and objectives. [PDF]
J Oral Biol Craniofac Res, 2022 Droubi L +3 more
europepmc +1 more source
Apert syndrome with omphalocele [PDF]
Journal of Perinatology, 2010 T E, Herman, M J, Siegel
openaire +2 more sources