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BMJ Open FO Journal:Manuscript ID:Article Type:Date Submitted by the Author:Complete List of Authors:BMJ Openbmjopen2012001917Research31Aug2012wieevrreeWildhardt, Gabriele; bio. Louis, Center of Human
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Begin by collecting detailed medical and family history to identify any patterns or recurring symptoms related to Waardenburg-Shah Syndrome (WS) type.
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Individuals presenting with symptoms such as hearing loss, changes in skin pigmentation, distinctive facial features, and abnormalities in the eyes may need to undergo testing for Waardenburg-Shah Syndrome (WS) type.
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Waardenburg-Shah syndrome type (WS) is a rare genetic disorder that is characterized by hearing loss, changes in pigmentation of the hair, skin, and eyes, and in some cases, Hirschsprung disease.
Medical professionals and researchers specializing in genetics are required to file waardenburg-shah syndrome ws type.
Waardenburg-Shah syndrome ws type can be filled out by providing detailed information about the patient's medical history, symptoms, and genetic testing results.
The purpose of waardenburg-shah syndrome ws type is to document and track cases of the syndrome for research, treatment, and diagnostic purposes.
Information such as patient demographics, family history, clinical symptoms, genetic testing results, and any other relevant medical information must be reported on waardenburg-shah syndrome ws type.
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