research APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.
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Hair TransplantHair Loss TreatmentsHSIIMoscow · RU - 18Hair Loss Treatments【医療提携サロン】ドライヘッドスパ・育毛促進専門店 SUI（スーパースカルプ松阪店）Ise · JP
- 64
Hair TransplantHair Loss TreatmentsHCI ClinicsUtrecht · NL - 50
Hair Loss TreatmentsSMPHCI Hair SolutionsLongwood, FL · US - 55
Hair TransplantHair Loss TreatmentsHS Hair ClinicLondon · GB - 35Hair TransplantSIYA ClinicsJaipur, Rajasthan · IN
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SMP SpecialistSue
Incomplete name
Preston, United Kingdom
- 55
TrichologistSue Hedrick
Sarasota, FL, United States
- 81
Hair Loss SpecialistDr. Zoya Rana, BDS, MDS, ABHRS
Muzaffarnagar, Uttar Pradesh, India
- 65
Hair Loss SpecialistZoe Passam
New York, NY, United States
- 87
DermatologistDr. A. Sai Sandeepthi, MD, MBBS
Serilingampalle, Telangana, India
- 63
SMP SpecialistSue Winter
Northampton, United Kingdom
Research
5 / 281 results 
research A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.
research Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach
Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.
research Hair: more than just an appendage
A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.
research Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy
Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.
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