Search

everythinglearnresearchcommunity

for

Search:↓

Facial hyperpigmentation improved with oral isotretinoin and ivermectin cream after Demodex mites were identified as the cause.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Women with PCOS in North China often have hirsutism and acne, with hirsutism linked to metabolic issues.

Most classic movie villains have skin conditions, unlike the heroes, which may cause bias against real people with similar conditions.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

People with pemphigus vulgaris and pemphigus foliaceus often have smaller sebaceous glands on their scalp.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Frontal Fibrosing Alopecia is a type of hair loss affecting mostly older women, with no agreed best treatment.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Hair bands are a new symptom of facio-genito-popliteal syndrome.

FFA in young women is often missed, and no single treatment works best.

Bumps on the face may be an early sign of a type of hair loss called frontal fibrosing alopecia.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

Hormonal therapy in adults with gender dysphoria often leads to skin issues like acne, requiring a team of skin and hormone doctors.

The study suggests hormonal factors may play a role in Frontal Fibrosing Alopecia and that treatments like oral antiandrogens and steroids could be beneficial.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Frontal fibrosing alopecia causes hair loss along the frontal hairline, mainly in postmenopausal women, and needs better treatments.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

A reliable severity score for female pattern hair loss was developed and validated.

Facial feminization surgery is safe and patients are satisfied, but more detailed research is needed.

Skin symptoms can indicate endocrine disorders and have various treatments.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A 59-year-old woman was diagnosed with a rare hair loss condition called lipedematous alopecia.

Antifungal treatment can improve severe skin infections with cutaneous horns.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.