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A man with hair loss developed a condition causing scarring and inflammation in both bald and non-bald areas of his scalp.

Tofacitinib helped a woman regrow her hair without relapses after other treatments failed.

Abrocitinib effectively treats severe alopecia areata with significant improvement and no side effects.

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

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Postmenopausal frontal fibrosing alopecia may be a unique condition linked to postmenopausal changes.

Tofacitinib works well for treating alopecia areata, especially when combined with corticosteroids, but is less effective if the disease has lasted over 2 years.

Autoimmune diseases like lupus, dermatomyositis, and scleroderma can cause hair loss and other hair problems, and treatments for these diseases might also affect hair.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Some people with Frontal Fibrosing Alopecia may be allergic to a common sunscreen ingredient.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

Mutations in the LIPH gene cause woolly hair in a child.

A rare ovarian tumor can cause unusual male-like symptoms, but surgery usually leads to a good outcome.

Baricitinib shows promise in improving frontal fibrosing alopecia symptoms.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Frontal fibrosing alopecia in Bogotá mainly affects postmenopausal women, with possible links to hormonal changes and sunscreen use.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

A woman had a skin condition with increased normal elastic fibers, not related to other known disorders, likely due to aging.

A high fat lard diet may protect against skin fibrosis and affect hair growth.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

A woman with lupus and antiphospholipid syndrome had bone damage, showing the need for careful treatment.

Fibroblasts are important in healing diabetic wounds, but high sugar levels can harm their function and slow down the healing process.

A unique type of hair loss mimics another condition but has minimal inflammation and specific immune cells present.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

Filgotinib completely reversed hair loss in a patient with rheumatoid arthritis and alopecia universalis.

Different types of fibroblasts play various roles in kidney repair and aging, and may affect chronic kidney disease outcomes.

The conclusion is that CD90 is not a specific marker for fibroblast subtypes and better methods are needed to identify them.

A rare case of a man having both frontal fibrosing alopecia and vitiligo was reported.