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Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

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

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

A new hair transplant method suggests freezing and storing dense hairs for future use to address severe hair loss.

FGF5 gene mutations cause long hair in domestic cats.

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

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

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

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

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.

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

A subtle androgen receptor abnormality can allow normal male development and sometimes fertility despite partial androgen resistance.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Genetic testing is crucial for diagnosing rare hair loss disorders.

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

Merkel cells may have roles in sensing magnetic fields, creating fingerprints, Reiki energy healing, passing on environmental information to offspring, and influencing hair shape.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

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

Pygmy goats with seborrhoeic dermatitis showed skin symptoms and temporary improvement with corticosteroids, but the cause and inheritance of the disease remain unknown.

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

Abnormal gene expression related to keratin causes hair loss in certain mice.