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Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [3] Many parts of the body are affected. [ 3 ] Babies are often born small and have heart defects . [ 3 ]
Triploid syndrome, also called triploidy, is a chromosomal disorder in which a fetus has three copies of every chromosome instead of the normal two. If this occurs in only some cells, it is called mosaic triploidy and is less severe. Most embryos with triploidy miscarry early in development.
Brittle-cornea syndrome is characterized by the progressive thinning of the cornea, early-onset progressive keratoglobus or keratoconus, nearsightedness, hearing loss, and blue sclerae. [5] [36] Classic symptoms, such as hypermobile joints and hyperelastic skin, are also seen often. [37] It has two types. Type 1 occurs due to variations in the ...
This page was last edited on 28 April 2023, at 21:46 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...
Ectrodactyly–ectodermal dysplasia–cleft syndrome; Edwards syndrome; EEM syndrome; Egg drop syndrome; Ehlers–Danlos syndrome; Eiken syndrome; Einstein syndrome; Eisenmenger's syndrome; Eldomery-Sutton syndrome; Elejalde syndrome; Ellis–van Creveld syndrome; Emanuel syndrome; Empty nest syndrome; Empty nose syndrome; Empty sella syndrome
Hypertelorism is a symptom in a variety of syndromes, including Edwards syndrome (trisomy 18), 1q21.1 duplication syndrome, basal cell nevus syndrome, DiGeorge syndrome and Loeys–Dietz syndrome.
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Cri-du chat syndrome; Schmid–Fraccaro syndrome; Turner's syndrome; Ring-D chromosome; Monosomy-G syndrome; Trisomy 13 (Patau's syndrome, D-syndrome) Trisomy 18 (Edwards' syndrome, E-syndrome) Trisomy 21 (Down syndrome) Deletion of long arm of chromosome 18; Deletion of chromosome 18
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related to: edwards syndrome symptoms