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*  Hypohidrotic ectodermal dysplasia
Affected individuals tend to have sparse scalp and body hair (hypotrichosis). The hair is often light-coloured, brittle, and ...
*  Hypotrichosis
... is a common feature of Hallermann-Streiff syndrome as well as others. It can also be used to describe the lack of ... The opposite of hypotrichosis is hypertrichosis, where terminal hair (thick) grows in areas that would otherwise normally have ... Hypotrichosis (hypo- + tricho- + -osis) is a condition of abnormal hair patterns, predominantly loss or reduction. It occurs, ... Genetic forms of localized autosomal recessive hypotrichosis include: List of conditions caused by problems with junctional ...
*  Marie Unna hereditary hypotrichosis
... (also known as "Marie Unna hypotrichosis") is an autosomal dominant condition characterized ...
*  Hypotrichosis-lymphedema-telangiectasia syndrome
... is a congenital syndrome characterized by lymphedema (swelling of tissue due ... and hypotrichosis or alopecia (hair loss). Lymphedema usually develops in the lower extremities during puberty. Hair is normal ... "Vascular defects in a mouse model of hypotrichosis-lymphedema-telangiectasia syndrome indicate a role for SOX18 in blood vessel ...
*  Hypotrichosis with juvenile macular dystrophy
... is an autosomal recessive hereditary disease. It is caused by a combination of ... Hypotrichosis with juvenile macular dystrophy (HJMD or CDH3) is an extremely rare congenital disease characterized by sparse ... "A Rare Syndrome: Hypotrichosis with Juvenile Macular Dystrophy (HJMD)". Investigative Ophthalmology & Visual Science. 55 (13): ... hair growth (hypotrichosis) from birth and progressive macular corneal dystrophy. Hair growth on the head is noticeably less ...
*  List of OMIM disorder codes
TSHR Hypotrichosis and recurrent skin vesicles; 613102; DSC3 Hypotrichosis simplex of scalp; 146520; CDSN Hypotrichosis, ... HR Hypotrichosis, localized, autosomal recessive 2; 604379; LIPH Hypotrichosis, localized, autosomal recessive, 3; 611452; ... P2RY5 Hypotrichosis, localized, autosomal recessive; 607903; DSG4 Hypotrichosis-lymphedema-telangiectasia syndrome; 607823; ... KRT10 Ichthyosis with hypotrichosis; 610765; ST14 Ichthyosis, congenital, autosomal recessive; 612281; ICHYN Ichthyosis, cyclic ...
*  Canine follicular dysplasia
"Hereditary Alopecia and Hypotrichosis". The Merck Veterinary Manual. 2006. Retrieved 2007-03-04. von Bomhard W, Mauldin E, ...
*  Corneodesmosin
2003). "Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin". Nat. Genet. ... "Entrez Gene: CDSN corneodesmosin". Toribio J, Quiñones PA (1975). "Hereditary hypotrichosis simplex of the scalp. Evidence for ...
*  Eyelash
"Bimatoprost in the treatment of eyelash hypotrichosis". National Institutes Of Health. 26 April 2010. Retrieved 2017-09-16. ...
*  Management of hair loss
They found the gene P2RY5 causes a rare, inherited form of hair loss called hypotrichosis simplex. It is the first receptor in ... Law, S. K. (2010). "Bimatoprost in the treatment of eyelash hypotrichosis". Clinical ophthalmology (Auckland, N.Z.). 4: 349-358 ...
*  Bimatoprost
The medical term for this is treatment of hypotrichosis; however, the FDA approval is for purely cosmetic purposes (see ...
*  Pure hair-nail type ectodermal dysplasia
Manifestations of this disorder include onychodystrophy and severe hypotrichosis. It represents as an autosomal dominant trait ...
*  60S ribosomal protein L21
Mutations in the RPL21 gene result in Hypotrichosis simplex of the scalp. GRCh38: Ensembl release 89: ENSG00000122026 - Ensembl ... March 2011). "Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex". Human Mutation. 32 (7): 710-4. doi ...
*  X-linked recessive inheritance
Hypohidrotic ectodermal dysplasia, presenting with hypohidrosis, hypotrichosis, hypodontia Kabuki syndrome; multiple congenital ...
*  Laboratory rat
Moemeka, A. N., Hildebrandt, A.L., Radaskiewicz, P., & King, T. R. (1998). Shorn (shn): a new mutation causing hypotrichosis in ...
*  Brazilian hair straightening
... hypotrichosis, chest pain, chest discomfort, emesis, and rash. Girard Gibbs' false advertising lawyers have filed a class ...
*  LIPH
2005). "A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3". J. Med. Genet. 41 (11): ... 2007). "A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis". Hum. Genet. 121 (3-4): 319-25. doi: ...
*  Desmoglein-4
2007). "Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive ... 2003). "Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and ... "A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis". J. ... "Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats". J. Investig. Dermatol. ...
*  Bazex-Dupré-Christol syndrome
Physical findings typically include follicular atrophoderma, multiple basal cell carcinomas, hypotrichosis, and hypohidrosis. ...
*  Cat skin disorders
These include skin fragility syndrome (Ehlers-Danlos), hereditary hypotrichosis and congenital or hereditary alopecia. Some ...
*  CDH3 (gene)
Mutations in this gene have been associated with congenital hypotrichosis with juvenile macular dystrophy. CDH3 (gene) has been ...
*  HR (gene)
Variations in this gene is involved in low levels of hair (baldness / alopecia / hypotrichosis) Mutations in this gene in ... "Identification of mutations in U2HR in two Chinese families with Marie Unna hereditary hypotrichosis". Clin Exp Dermatol. 41 (2 ...
*  Telangiectasia
"Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema- ... meningeal angiomas and mental retardation Hypotrichosis-lymphedema-telangiectasia syndrome, caused by mutation in transcription ...
*  Schöpf-Schulz-Passarge syndrome
... (also known as "eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis") is an ... In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts ( ... hypodontia and hypotrichosis as a possible autosomal recessive trait". Birth Defects Orig. Artic. Ser. 7 (8): 219-21. PMID ...