Search

everythinglearnresearchcommunity

for

Search:↓

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.

PCOS may be influenced by factors in the blood, not just the ovaries.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

Certain gene variations may increase the risk and severity of alopecia areata.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A new gene mutation causes insulin resistance in a girl and her mother.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Vitiligo is often found with other autoimmune diseases, which is important to know to help patients.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.