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apert
apert, a. and adv. arch. (əˈpɜːt) Also 4–6 appert, and aphet. pert. [a. OFr. apert:—L. apert-um open, pa. pple. of aperī-re to open: see aperient. In OFr. the word was to some extent confused with aspert = espert:—L. expertus, ‘expert,’ which seems to have affected some of the senses.] A. adj. 1. Op...
Oxford English Dictionary
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Apert
Apert is a forested mountain, , in the western Volcanic Eifel, a mountain range in the German state of Rhineland-Palatinate. Geology
The region is part of the Rhenish Massif; the basement of the Apert consists of the fossil-rich Büdesheim Slate and Flinz, a rock of the lower
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Eugène Apert
Eugène Charles Apert (27 July 1868 – 2 February 1940) was a French pediatrician born in Paris. References
External links
Eugène Charles Apert @ Who Named It
Dermatology Online Journal Apert syndrome
French pediatricians
1868 births
1940 deaths
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aperté
† aperté Obs. rare—1. [a. OFr. aperté military skill, f. apert expert: see prec.] The public manifestation of skill; display of prowess.1470 Harding Chron. cxcviii, Consyderyng well his knightly aperte.
Oxford English Dictionary
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Apert syndrome
This is the most uncommon but also most severe form of hand deformity in Apert syndrome. This may explain why both symptoms are always found in Apert syndrome.
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appertise
▪ I. † appertise, -yse, n. Obs. [a. OFr. appertise, -artise (mod. apertise), f. apert open, manifest: see apert 4.] Open display, proof, or evidence of dexterity, skill, or valour, esp. in arms.1480 Caxton Ovid's Met. xi. xxii, He was wyse, dyscrete, and ful of al appertyse. 1485 ― Paris & V. 10 Non...
Oxford English Dictionary
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Andrew Wilkie (geneticist)
He identified the gene mutation responsible for Apert syndrome and the molecular pathways underlying this and other craniosynostosis conditions. Wilkie's discovery that the mutation causing Apert syndrome was more common than expected led him to develop the 'selfish selection' theory, which states
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Childhood tumor syndrome
See also
Apert syndrome
List of cutaneous conditions
References
Genodermatoses
Syndromes
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亞伯氏症候群Apert Syndrome - 長庚兒童整形顱顏外科 盧亭辰醫師
愛伯氏症候群(Apert Syndrome)治療. 罕見的先天性疾病,由於顱縫早期閉合引起顱骨異常和併指的一種先天性綜合徵,顱骨呈現又扁又高,多為兩側冠狀縫過早閉合, 有時合併額狀縫癒合. 手指全黏在一起,尤以第2、3指最易受到侵犯,合併程度從皮膚、軟組織到 ...
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Apert综合征_百度百科
Apert综合征又称为尖头并指综合征(acrocephalosyndactyly),为散发的常染色体显性遗传性疾病,是以尖头、短头、面中份发育不良及并指(趾)为特征的一组症候群。颅面部的症状与Crouzon综合征相似,表现为颅缝早闭所致的头颅畸形、突眼和面中部严重发育不良。在Apert综合征中,头颅畸形多为尖头和短头 ...
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Acrocephalosyndactyly
There has been a case of a prenatal diagnosis of Apert syndrome using fetoscopy. In more severe subtypes, as seen in Apert syndrome, surgical correction of syndactyly may be needed.
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Craniosynostosis, Philadelphia type
The syndactyly was mitten-like and resembled Apert syndrome but was excluded as being caused by Apert syndrome due to the lack of bony involvement.
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