Apert Syndrome: An Insight Into Dentofacial Features. [PDF]
Cureus, 2021 Jose B +4 more
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Craniofacial morphology in Apert syndrome: a systematic review and meta-analysis. [PDF]
Sci Rep, 2022 Alam MK +5 more
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Gallbladder Hypoplasia With Intestinal Malrotation in a Patient With Apert Syndrome: A Case Report. [PDF]
Case Rep SurgEaswaran L, Vincent SA, Diaz-Miron JL.
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Apert syndrome: an informative long-term dentofacial outcome. [PDF]
BMJ Case Rep, 2022 Fowler P, Hallang S, Snape L.
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Long-term survival without high cancer risk in a cohort of 24 patients with Apert syndrome. [PDF]
Eur J Hum GenetCairns BJ +3 more
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Acrocephalosyndactyly Type 1 (Apert Syndrome): A Case Report. [PDF]
Indian Dermatol Online J, 2021 Chavda V, Shah A, Chaudhari D.
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Early Motor Development and Rehabilitation Outcomes in Apert Syndrome: Gross Motor Function Measures-Case Report. [PDF]
PathophysiologyOreščanin L, Biloglav Z, Škrlec I.
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Paediatrica Indonesiana, 1993 A case of Apert syndrome in a male child of 5 months old has been reported. The diagnosis was based on the clinical appearance (phenotype) showing acrocephaly and syndactyly of both hands and feet, supported by skull roentgenography and ultrasonography. The patient was the third child from normal parents, and the two other children were normal.
Wenger TL, Hing AV, Evans KN.
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Diagnosing fetal apert syndrome: a case study on prenatal diagnosis and genetic insights. [PDF]
Quant Imaging Med SurgGe T +8 more
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Prenatal diagnosis of Apert syndrome with continuation of pregnancy-a report of two cases. [PDF]
Transl PediatrVida MVG +6 more
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