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PCOS and related metabolic issues often run in families.

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

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.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

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

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.

Hair loss in certain mice is linked to changes in keratin-related genes.

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.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

FGF5 gene mutations cause long hair in domestic cats.

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

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

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

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

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.

Some families have a genetic condition where they are born with irregular scalp defects.

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

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.

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

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

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.

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.

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.

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

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

A girl inherited excessive body hair from her mother and grandmother.