×
About 924 results

ALLMedicine™ Hypotrichosis Center

Research & Reviews  453 results

Further phenotypic features and two novel POC1A variants in a patient with SOFT syndrom...
https://doi.org/10.3892/mmr.2021.12133
Molecular Medicine Reports; Li S, Zhong Y et. al.

May 6th, 2021 - Short stature, onychodysplasia, facial dysmorphism and hypotrichosis (SOFT) syndrome is a rare autosomal recessive disease caused by POC1 centriolar protein A (POC1A) pathogenic variants. However, knowledge of genotypic and phenotypic features of ...

Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated wi...
https://doi.org/10.1002/ajmg.a.62205
American Journal of Medical Genetics. Part A; Coulie R, Niyazov DM et. al.

Apr 14th, 2021 - Hypotrichosis-lymphedema-telangiectasia syndrome (HLTS) is a rare condition caused by pathogenic variants in the SOX18 gene. SOX18 plays a key role in angio- and lymphangiogenesis due to its expression in venous endothelial cells from which the ly...

The first Japanese family of CDH3-related hypotrichosis with juvenile macular dystrophy.
https://doi.org/10.1002/mgg3.1688
Molecular Genetics & Genomic Medicine; Hayashi T, Katagiri S et. al.

Apr 10th, 2021 - Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare autosomal recessive inherited disorder caused by biallelic variants in the CDH3 gene encoding P-cadherin. Here, we report two Japanese sibling patients with HJMD. Whole-exome sequencin...

Revisiting the Safety of Prostaglandin Analog Eyelash Growth Products.
https://doi.org/10.1097/DSS.0000000000002928
Dermatologic Surgery : Official Publication for American ... Steinsapir KD, Steinsapir SMG

Feb 24th, 2021 - The FDA approved bimatoprost ophthalmic solution 0.03% for treatment of eyelash hypotrichosis in 2008. Consumer concern persists regarding potential side effects of this product. To identify gaps in the safety information associated with the use o...

No evidence for preferential X-chromosome inactivation as the main cause of divergent p...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901220
Orphanet Journal of Rare Diseases; Körber L, Schneider H et. al.

Feb 24th, 2021 - X-linked hypohidrotic ectodermal dysplasia (XLHED), a rare genetic disorder, affects the normal development of ectodermal derivatives, such as hair, skin, teeth, and sweat glands. It is caused by pathogenic variants of the gene EDA and defined by ...

see more →

Drugs  5 results see all →

Clinicaltrials.gov  463 results

Further phenotypic features and two novel POC1A variants in a patient with SOFT syndrom...
https://doi.org/10.3892/mmr.2021.12133
Molecular Medicine Reports; Li S, Zhong Y et. al.

May 6th, 2021 - Short stature, onychodysplasia, facial dysmorphism and hypotrichosis (SOFT) syndrome is a rare autosomal recessive disease caused by POC1 centriolar protein A (POC1A) pathogenic variants. However, knowledge of genotypic and phenotypic features of ...

Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated wi...
https://doi.org/10.1002/ajmg.a.62205
American Journal of Medical Genetics. Part A; Coulie R, Niyazov DM et. al.

Apr 14th, 2021 - Hypotrichosis-lymphedema-telangiectasia syndrome (HLTS) is a rare condition caused by pathogenic variants in the SOX18 gene. SOX18 plays a key role in angio- and lymphangiogenesis due to its expression in venous endothelial cells from which the ly...

The first Japanese family of CDH3-related hypotrichosis with juvenile macular dystrophy.
https://doi.org/10.1002/mgg3.1688
Molecular Genetics & Genomic Medicine; Hayashi T, Katagiri S et. al.

Apr 10th, 2021 - Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare autosomal recessive inherited disorder caused by biallelic variants in the CDH3 gene encoding P-cadherin. Here, we report two Japanese sibling patients with HJMD. Whole-exome sequencin...

Revisiting the Safety of Prostaglandin Analog Eyelash Growth Products.
https://doi.org/10.1097/DSS.0000000000002928
Dermatologic Surgery : Official Publication for American ... Steinsapir KD, Steinsapir SMG

Feb 24th, 2021 - The FDA approved bimatoprost ophthalmic solution 0.03% for treatment of eyelash hypotrichosis in 2008. Consumer concern persists regarding potential side effects of this product. To identify gaps in the safety information associated with the use o...

No evidence for preferential X-chromosome inactivation as the main cause of divergent p...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901220
Orphanet Journal of Rare Diseases; Körber L, Schneider H et. al.

Feb 24th, 2021 - X-linked hypohidrotic ectodermal dysplasia (XLHED), a rare genetic disorder, affects the normal development of ectodermal derivatives, such as hair, skin, teeth, and sweat glands. It is caused by pathogenic variants of the gene EDA and defined by ...

see more →

News  3 results

Hereditary Hypotrichosis Simplex of the Scalp
https://www.mdedge.com/dermatology/article/143213/hair-nails/hereditary-hypotrichosis-simplex-scalp
Ronda S. Farah, MD, Heather M. Holahan, MD et. al.

Jul 25th, 2017 - To the Editor: Hereditary hypotrichosis simplex (HHS)(Online Mendelian Inheritance in Man [OMIM] 146520) is a rare form of hypotrichosis that typically presents in school-aged children as worsening hair loss localized to the scalp. 1 Most patients.

Bimatoprost Approved for Eyelash Lengthening
https://www.mdedge.com/dermatology/article/9616/aesthetic-dermatology/bimatoprost-approved-eyelash-lengthening
Elizabeth Mechcatie

The Food and Drug Administration has approved bimatoprost for increasing the growth of eyelashes, a side effect of the glaucoma-treating drug that was first observed several years ago in clinical trials. The new indication for bimatoprost 0.

Hereditary Basaloid Follicular Hamartoma Syndrome
https://www.mdedge.com/dermatology/article/67384/nonmelanoma-skin-cancer/hereditary-basaloid-follicular-hamartoma-syndrome
Lee PL, Lourduraj LT et. al.

Basaloid follicular hamartoma (BFH) is a benign adnexal tumor consisting of basaloid cells with follicular differentiation. BFH can occur as a solitary lesion, multiple lesions, or an autosomal dominant inherited syndrome—BFH syndrome (BFHS).

see more →