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Absent skin pigmentation
- Epidermolysis Bullosa (National Institute of Arthritis and Musculoskeletal and Skin Diseases)Skin Conditions/Specifics ... Skin Conditions ... National Institute of Arthritis and Musculoskeletal and Skin Diseases ... From the National Institutes of Health ... Epidermolysis ...
- ... of the gene, the snail 2 protein is absent. Lack of snail 2 may disrupt the development of melanocytes in certain areas of the skin, hair, eyes, and inner ear, leading to hearing loss and the patchy loss of pigmentation that are characteristic features of Waardenburg syndrome type ...
- ... distinctive facial features, sparse hair, areas of unusual skin coloring (pigmentation), and other birth defects.Most babies with Pallister- ...
- ... condition also affects the eyes, teeth, hands, and skin coloring (pigmentation). Although many different medical issues have been associated ...
- ... congenita. This disorder is characterized by changes in skin coloring (pigmentation), white patches inside the mouth (oral leukoplakia), and ...
- ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
- ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
- ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...
- ... people with CMMRD syndrome also develop changes in skin coloring (pigmentation), similar to those that occur in a condition ...