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Exposure to the hair loss drug finasteride during pregnancy can cause genital anomalies in male babies, but not in female babies. It's best to avoid this drug in women who could potentially become pregnant.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

Some people with congenital triangular alopecia have a central tuft of hair in the bald patch, but the cause is unknown.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A new technique effectively treats and diagnoses eruptive vellus hair cysts without recurrence.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

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

Too much Sonic Hedgehog protein stops hair growth in embryos.

Polarized microscopy helps identify hair irregularities in genetic disorders.

Gamma-ray exposure during hair rest phase harms hair growth and color in mice.

Hair changes can indicate systemic diseases or medication effects.

Bleaching and UV exposure significantly damage hair.

Health issues in retired breeder guinea pigs don't affect experiment success.

HLD10 can include increased body hair and Mongolian spots.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

The hair defect is due to abnormal inner root sheath keratinization.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Oral minoxidil improved hair thickness in a person with monilethrix.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Acanthus montanus extract harms fetal development and causes infertility in offspring.

Some men with early hair loss may have a condition similar to PCOS in women.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.