Pubmed is a searchable database of medical literature and lists journal articles that discuss mohrtranebjaerg syndrome. Phenotypic and molecular characterisation of the aarskogscott syndrome. Caracterizacion fenotipica del sindrome aarskog medigraphic. Phenotype and molecular characterisation of aarskogscott syndrome.
Click on the link to view a sample search on this topic. Aarskog scott syndrome is a genetic disorder that affects the development of many parts of the body. Pdf the phenotypic fndings of 7 patients who were diagnosed aarskog syndrome in the. Aarskogscott syndrome aas is a rare developmental disorder which primarily affects males and has a relative prevalence of 1 in. Aarskog syndrome nord national organization for rare disorders. People with aarskog scott syndrome often have distinctive facial features, such as widely spaced eyes hypertelorism, a small nose, a long area between the nose and mouth philtrum, and a widows. Os portadores caracterizamse pela baixa estatura e por anormalidade faciais, esqueleticas e genitais. Please use one of the following formats to cite this article in your essay, paper or report.
Enable javascript to view the expandcollapse boxes. This condition mainly affects males, although females may have mild features of the syndrome. Aarskog syndrome also known as aarskogscott syndrome,faciodigitogenital syndrome or faciogenital dysplasia is a rare,xlinked disorder predominantly affecting males,characterized by facial. Mohrtranebjaerg syndrome genetic and rare diseases. Attentiondeficit hyperactivity disorder adhd and its earlier nosologic classifications have been extensively investigated since the 1960s, with pubmed listings alone exceeding,000 entries.