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The document explains the genetic causes and characteristics of inherited hair disorders.

Hair transplant using beard hair made acne scars on cheeks less visible with minimal scarring in the donor area.

The conclusion is that effectively treating hair disorders is difficult due to the complex factors affecting hair growth and more research is needed to improve treatments.

A man had a benign pilar cyst on his face, which is rare and was successfully removed by surgery.

Certain health conditions and hair care habits affect the treatment results for a scalp condition called Central Centrifugal Cicatricial Alopecia.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.

Adult earlobe can have a benign cyst that is usually removed by surgery.

Trichobiolight effectively treats hair loss with 82.5% success.

A unique case showed a rare combination of two types of lichen planus on the face.

Triple horizontal scalp biopsies are 98% accurate in diagnosing hair loss, better than single biopsies.

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

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Lichen planopilaris can be accurately diagnosed and effectively treated.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Finasteride increases hair count and improves hair growth with low risk of side effects.

Frontal Fibrosing Alopecia is a slowly progressing hair loss condition, likely underdiagnosed, with ineffective treatments, needing more research to understand it fully.

Low level laser therapy is effective and safe for various skin and hair conditions.

Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

EZH2 levels decrease as fetuses develop and are higher in adult skin, which may affect skin growth and repair.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

A young tapir with a rare skin condition improved after treatment with wound cleaning, cream, and oral medication.

Some factors like thyroid disease, diabetes treatment, hair dryers, natural hairstyles, and scalp conditions can affect the treatment results for a hair loss condition called CCCA.

IL-33 is linked to hair follicle damage in psoriasis and could be a treatment target for hair loss in this condition.

Two young cats with a severe ear and skin condition improved with immune system-targeting treatments.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

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

A rare benign skin nodule was found on the buttock, a unique location for this condition.

A woman had a rare, non-cancerous skin growth on her face, which was removed and did not come back after a year.

A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.