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Combination therapy with steroids and pimecrolimus improved or stabilized hair loss in most patients with Frontal Fibrosing Alopecia, who also had a high rate of hypothyroidism.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

Early combination therapy can effectively regrow hair in frontal fibrosing alopecia.

The Foxn1 gene is essential for normal nail and hair development.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Fetal exposure to diazoxide can cause hair loss and abnormal hair growth in infants.

ALRN-6924 may prevent hair loss caused by chemotherapy.

FoxA is crucial for pharynx regeneration in planarian flatworms.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Lhx2 helps retinal cells respond to signals for eye development.

Low-dose naltrexone helps improve symptoms and stabilize frontal fibrosing alopecia and lichen planopilaris.

Experts agreed on guidelines to improve research on Frontal Fibrosing Alopecia.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Forehead reduction and orbital contouring are important for satisfactory facial feminization in transgender females, with high satisfaction and low long-term problems.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

The (bi)eyebrow approach is better for frontal sinus injuries, reducing scarring and complications.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Oral isotretinoin effectively treats yellow facial papules in frontal fibrosing alopecia patients.

A child with rough nails also had hair loss and allergies.

Being allergic to linalool, a common fragrance ingredient, might contribute to developing frontal fibrosing alopecia.

Two young siblings experienced hair loss without hormone issues or other skin problems.

Phospholipase C-δ1 is crucial for normal hair development.

Inhibiting Zyxin may help treat androgenetic alopecia by promoting hair growth.

Mutations in specific genes cause different types of ectodermal dysplasias.

Certain gene variations increase the risk of alopecia areata in Koreans.