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WEWALK

NEWBURY PARK-USA

Company Name:
Corporate Name:
WEWALK
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Company Address: 1125 Business Center Circle,NEWBURY PARK,CA,USA 
ZIP Code:
Postal Code:
91319 
Telephone Number: 8055012399 (+1-805-501-2399) 
Fax Number: 8054992964 (+1-805-499-2964) 
Website:
 
Email:
 
USA SIC Code(Standard Industrial Classification Code):
738999 
USA SIC Description:
Business Services Nec 
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  • Waardenburg syndrome - Wikipedia
    Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin
  • Waardenburg Syndrome: Symptoms Causes - Cleveland Clinic
    Waardenburg syndrome is a genetic condition that causes changes to the coloring (pigmentation) of your hair, eyes and skin and can cause hearing loss in some people
  • Waardenburg syndrome | About the Disease | GARD
    Waardenburg syndrome (WS) is a group of genetic conditions characterized by varying degrees of hearing loss and differences in the coloring (pigmentation) of the eyes, hair, and skin Signs and symptoms can vary both within and between families Various other features may also be present
  • Waardenburg Syndrome - Symptoms, Causes, Treatment | NORD
    Waardenburg syndrome is a genetic disorder that may be evident at birth (congenital) The range and severity of associated symptoms and findings may vary greatly from case to case
  • What Should You Know About Waardenburg Syndrome? - WebMD
    Waardenburg syndrome is a genetic condition that affects the color of your hair, skin, and eyes and can also cause hearing loss and gastrointestinal issues There's no cure, but your doctor can
  • Waardenburg Syndrome Symptoms, Types, and Treatment
    Waardenburg syndrome is a rare genetic disorder that can cause deafness and changes in skin, hair, and eye color It is passed down in an autosomal dominant pattern, giving affected individuals a 50% chance of having an affected child
  • Waardenburg syndrome Information | Mount Sinai - New York
    Learn about Waardenburg syndrome, find a doctor, complications, outcomes, recovery and follow-up care for Waardenburg syndrome
  • Waardenburg syndrome - Orphanet
    WS accounts for 2-5% of congenital hearing loss and affects all ethnic groups without gender differences WS2 is the most common subtype, followed by WS1 Clinical manifestations vary within and between families
  • Waardenburg Syndrome - StatPearls - NCBI Bookshelf
    Waardenburg syndrome is a group of genetic conditions inherited in an autosomal dominant fashion During embryogenesis, there is an abnormal distribution of melanocytes, which results in patchy areas of depigmentation
  • Waardenburg syndrome: MedlinePlus Genetics
    Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes Although most people with Waardenburg syndrome have normal hearing, moderate to profound hearing loss can occur in one or both ears




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