Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Digit ratio likely doesn't predict male hair loss.

Black dots under trichoscopy can appear in different hair and scalp conditions, not just in alopecia areata.

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.

Ultrasound biomicroscopy is useful for viewing hair follicles in alopecia areata.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

The study found that Temporal Triangular Alopecia often starts in early childhood, mainly affects the left side of the scalp, and has no effective treatment except surgery.

UVF-dermoscopy is a useful tool for accurately diagnosing types of alopecia, especially in people with lighter skin.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Segmented hair color changes can indicate active alopecia areata.

Using both trichoscopy and folliscopy together improves hair loss diagnosis in men.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

The "color-transition sign" helps tell apart alopecia areata incognita from telogen effluvium by looking at hair color changes.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Dupilumab improved hair and skin in a woman with Netherton syndrome.

Temporal triangular alopecia is a non-scarring hair loss seen in some Asian children.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

A new type of alopecia areata, called the "confetti variant," causes small bald spots that often heal on their own in a few months.

The study concluded that neonatal occipital alopecia is common, not caused by physical friction, and usually resolves on its own without treatment.

Two key genetic areas linked to male-pattern baldness were identified.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Yellow dots are common in severe alopecia areata.

Some women with PCOS have rare genetic variants linked to the condition.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Using both vertical and transverse sections for alopecia biopsies improves diagnosis without extra cost.