Apert syndrome
(ă-pār′)
[Eugene Apert, Fr. pediatrician, 1868-1940]
A congenital condition marked by premature closure of the sutures of the skull causing malformations of the head. Other manifestations include webbed fingers and toes, cleft palate or uvula, prognathic mandible, and maxillary hypoplasia, resulting in extreme malocclusion. It is sometimes mistakenly called Alpert syndrome.
Citation
Venes, Donald, editor. "Apert Syndrome." Taber's Medical Dictionary, 24th ed., F.A. Davis Company, 2021. Nursing Central, nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/767984/all/Apert_syndrome.
Apert syndrome. In: Venes DD, ed. Taber's Medical Dictionary. F.A. Davis Company; 2021. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/767984/all/Apert_syndrome. Accessed December 20, 2024.
Apert syndrome. (2021). In Venes, D. (Ed.), Taber's Medical Dictionary (24th ed.). F.A. Davis Company. https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/767984/all/Apert_syndrome
Apert Syndrome [Internet]. In: Venes DD, editors. Taber's Medical Dictionary. F.A. Davis Company; 2021. [cited 2024 December 20]. Available from: https://nursing.unboundmedicine.com/nursingcentral/view/Tabers-Dictionary/767984/all/Apert_syndrome.
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