Results 111 to 120 of about 5,209 (186)
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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Craniofacial manifestations of Loeys Dietz syndrome : A case report and a review of the literature : Case report [PDF]
, 2015 症例報
Hosokawa, Ko +4 more
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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
Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers. [PDF]
Cureus, 2023 Kumari K +10 more
europepmc +1 more source
Apert Syndrome: New Treatment and a Perspective for the Future [PDF]
, 2015 Treatment the Apert Syndrome is unique, therefore, divergences exist in the priority of the procedures performed by each team. The Apert Syndrome occurs in approximately 1/65,000 births and accounts for 4.5% of all craniosynostosis. Some changes in Apert
Barbosa do Nascimento, Vânia +9 more
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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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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
Abnormal mandibular growth and the condylar cartilage [PDF]
, 2017 Deviations in the growth of the mandibular condyle can affect both the functional occlusion and the aesthetic appearance of the face. The reasons for these growth deviations are numerous and often entail complex sequences of malfunction at the cellular ...
Luder, Hans. U. +3 more
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