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Apert Syndrome | Boston Children's Hospital
Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones . It is characterized by deformities of the skull, face, teeth, and limbs. www.childrenshospital.org
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Apert Syndrome: What Is It, Symptoms, Diagnosis & Treatment
Apert syndrome is a rare genetic condition that causes a baby's skull, face, feet and hands to form atypically when the skull joints close too soon. my.clevelandclinic.org
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Apert syndrome: MedlinePlus Genetics
Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure of the bones of the ... medlineplus.gov
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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 Syndrome | Children's Hospital of Philadelphia
Apert syndrome is a genetic disease affecting the shape of the head and face that also includes anomalies of the limbs and hands. www.chop.edu
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Apert Syndrome - StatPearls - NCBI Bookshelf
Apert syndrome, also known as acrocephalosyndactyly type I, is a genetically inherited syndrome characterized by multisuture craniosynostosis, midface ... www.ncbi.nlm.nih.gov
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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 wikipedia.org
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Apert Syndrome - Symptoms, Causes, Treatment | NORD
Apert syndrome is a rare genetic condition that is apparent at birth. People with Apert syndrome can have distinctive malformations of the skull ... rarediseases.org
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Apert Syndrome - Hand - Orthobullets
Syndrome characterized by bilateral complex syndactyly of hands and feet index, middle, and ring fingers. www.orthobullets.com
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Apert Syndrome: Background, Pathophysiology, Etiology
Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and severe symmetrical syndactyly. emedicine.medscape.com
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Apert syndrome - Wikipedia
Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. en.wikipedia.org
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Apert Syndrome | Children's Hospital Colorado
Apert syndrome, also known as acrocephalosyndactyly, is a condition characterized by abnormalities of the skull, midface and limbs. www.childrenscolorado.org
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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 wikipedia.org
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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. wikipedia.org
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