Search

everythinglearnresearchcommunity

for

Search:↓

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The CORIN gene variant causes the golden color in Siberian cats.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Antioxidants and growth factors may help treat hair loss when combined with LED and Laser therapy.

PCOS is caused by both genetics and environmental factors like diet and obesity.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Genes and hormones cause hair loss, with four genes contributing equally.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Advances in genetics may lead to targeted treatments for hair disorders.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Antifungal treatment can improve severe skin infections with cutaneous horns.

The document says that hair loss in women is often due to androgenic alopecia, similar to male baldness, and that hirsutism is treated with hormonal and cosmetic methods.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A rare skin condition causes red and dark patches on the face and limbs.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.