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Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Understanding and managing side effects of hedgehog pathway inhibitors can improve treatment for advanced basal cell carcinoma.

Newborn screening for biotinidase deficiency is effective in preventing severe complications.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Children with partial biotinidase deficiency are healthy at birth but may develop symptoms that improve with biotin therapy.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

The Hair Diameter Index (HDI) was created to help plan hair restoration surgery after finding that visual hair density is linked to hair count and thickness, not volume.

Hair follicle stem cells might help treat traumatic brain injury.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

The treatment effectively reduces hair loss and improves hair growth with minimal side effects.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Betulinic acid can help treat hepatitis C by stopping virus replication.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Bikunin is found on the cell boundaries of certain skin layers and may help regulate skin and hair functions.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Biotin supplements significantly improved a young girl's uncombable hair.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

People with Hidradenitis Suppurativa have less diverse skin bacteria and different bacterial metabolism than healthy individuals.