Search

everythinglearnresearchcommunity

for

Search:↓

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Cholesterol transport in hair follicles decreases from growth to regression phase.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Lack of cystatin M/E causes thin hair and dry skin.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Acitretin helped improve hand mobility and skin condition in a patient.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A gene variant causes a skin and hair disorder by disrupting protein balance.

New genetic variants linked to inherited ichthyoses were identified, offering insights for potential gene therapy.

Xiaozhi Yufa decoction may help treat hair loss by improving hair growth and reducing inflammation.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Disulfide bonds affect the melting behavior of hair's crystalline structure, but hair retains some stability even after these bonds are broken.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Changing disulfide bonds in human hair affects its melting behavior and thermal stability.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition that may respond to antiandrogen therapy.

FFA and FAPD might be related or stages of the same disease.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition with inflammation and scarring, resembling but distinct from common balding.

FAPD is a possible diagnosis for hair loss in patients of color and requires multiple evaluations for accurate diagnosis.

Fibrosing alopecia in a pattern distribution is a type of hair loss that may often be overlooked, especially in men.

Fibrosing alopecia in a pattern distribution is a new type of scarring hair loss that resembles common baldness and an autoimmune skin disease.

FAPD and possibly CCCA may be AGA subtypes, and treatments combining antiandrogens, hair growth agents, hair transplants, and anti-inflammatories could be effective.

FAPD in children may not depend on androgens and should be treated with anti-inflammatory measures and minoxidil.

Fibrosing alopecia in a pattern distribution is a hair loss condition often confused with other types, requiring early treatment but usually not resulting in significant hair regrowth.

A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.