Search

everythinglearnresearchcommunity

for

Search:↓

Managing frontal fibrosing alopecia and lichen planus pigmentosus is challenging due to resistant hair loss and skin discoloration.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Researchers found a gene mutation responsible for a rare hair loss condition.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Lavender oil use in a child may be linked to early puberty signs and elevated tumor marker levels.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Hidradenitis suppurativa improves with antiandrogen therapy.

Most treatments for Frontal Fibrosing Alopecia are ineffective, but early anti-inflammatory therapy may help and the condition may stabilize over time.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The document concludes that post-menopausal frontal fibrosing alopecia is a poorly understood condition that does not respond well to common treatments.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Different skin cells process testosterone differently, and certain drugs can change this process, possibly helping treat acne and hair loss.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

Treatment restored normal sexual characteristics and blood condition in a patient with testicular cancer.

Stopping steroids and providing supportive care improved the patient's Cushing Syndrome symptoms and ulcers.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

Women with hyperandrogenism have higher androgen levels and lower SHBG, which may contribute to conditions like excessive hair growth and early puberty.

Oral dutasteride and topical pimecrolimus can safely and effectively treat Frontal Fibrosing Alopecia, leading to significant hair regrowth.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

Early diagnosis and treatment with Leuprolide are key for children with precocious puberty.

The woman was diagnosed with lichen planopilaris and can be treated with corticosteroids.

Thallium, mercury, selenium, and colchicine strongly cause hair loss.

Plant extracts like Avicennia marina, Boehmeria nipononivea, and Camellia sinensis could potentially treat hair loss with fewer side effects than synthetic drugs.

Tofacitinib, a medication for arthritis, showed potential for treating severe hair loss in a small Brazilian case series, but more research is needed.

Male pattern baldness involves genetics, hormones, and needs better treatments.

DHT, a testosterone byproduct, causes male pattern baldness.

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

AGA can occur in children with family history; early diagnosis and treatment important.