Number of the records: 1
piebaldizmus
Record number d016116 Date 06.06.2025 Type M - MESH Topical term piebaldizmus Other term English (Pseudonym) Albinism, Cutaneous
English (Pseudonym) Albinism, Partial
Slovak (Pseudonym) pieboldizmus
Slovak (Pseudonym) albinizmus ohraničený
Slovak (Pseudonym) albinismus circumscriptus
Slovak (Pseudonym) albinizmus čiastočný
Slovak (Pseudonym) depigmentácie kože ohraničené
See also (Later heading) Waardenburgov syndróm
(Skutočné meno) Waardenburgov syndróm
(Later heading) proteíny protoonkogénové c-kit
UDC C16.320.290.040.600C16.320.565.100.102.600C16.320.850.080.600C17.800.621.440.102.600C17.800.827.080.600C18.452.648.100.102.600 Note Autosomal dominant, congenital disorder characterized by localized hypomelanosis of the skin and hair. The most familiar feature is a white forelock presenting in 80 to 90 percent of the patients. The underlying defect is possibly related to the differentiation and migration of melanoblasts, as well as to defective development of the neural crest (neurocristopathy). Piebaldism may be closely related to WAARDENBURG SYNDROME. subject heading
Number of the records: 1