American Academy of Pediatrics. Facial Dysmorphism. American Academy of Pediatrics; ;. For full access to this content, please log in to an existing user account or purchase an individual subscription.
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Dysmorphic features in Congenital Dysorders
Aka: Dysmorphic features in Congenital Dysorders. These images are a random sampling from a Bing search on the term "Dysmorphic features in Congenital Dysorders. Search Bing for all related images. Started in , this collection now contains interlinked topic pages divided into a tree of 31 specialty books and chapters. Content is updated monthly with systematic literature reviews and conferences. Although access to this website is not restricted, the information found here is intended for use by medical providers.
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PubMed Central. Peroxisomal disorders are a group of genetically heterogeneous metabolic diseases related to dysfunction of peroxisomes. Dysmorphic features , neurological abnormalities, and hepatic dysfunction can be presenting signs of peroxisomal disorders. Here we presented dysmorphic facial features and other clinical characteristics in two patients with PEX1 gene mutation.
In this section, drawings are used to depict terminology and to illustrate certain aspects of facial variation. Many features of the face that are considered abnormal are continuous, quantitative traits, plotting above or below 2 S. A continuous trait, like ear size, is quite different from a discontinuous trait such as a pre-auricular ear pit since an ear pit is considered either present or absent figure below. Thus, there is usually no disagreement among physicians as to whether an ear pit is present or not.