Factors Risk Aarskog Of A Syndrome - Defect

Factors Risk Aarskog of a syndrome - defect comes to light more often at men though women as can have more moderate displays of disease. (AF1). This syndrome is connected with mutations in a gene by name of FGDY1 which is found in X chromosome (Gene Map Locus: Xp11.21 (300546)).Faciogenital Dysplasia; Faciodigitogenital Syndrome, Aarskog Syndrome (from OMIM); Aarskog syndrome by oso.com Aase a syndrome, sin. - Aase-Smith 1 syndrome; Aase a syndrome rare the inherited defect characterised by an anaemia and skeletal uglinesses (http://www. ncbi. nlm. nih. gov / entrez/). Genetic localisation of illness is not known. The anaemia is caused structures and marrow functions. ABCD a syndrome (albinism, Black Lock, Cell Migration Disorder of the Neurocytes of the Gut, and Deafness), etc. Abdergaldena-Fankoni a syndrome, (-253.3); (.Abderhalden, 1877-1950, G.Fanconi, 1892-1979), . - Abdergaldena - Fankoni illness, ; , and , etc. (Abderhalden - Kaufmann - Lignac syndrome), a syndrome of Abdergaldena - Kaufmana - Ligna, Syndrome "Fankoni, a diathesis, a diabetes, , Nephritic gliko-amino-phosphatic diabetes.