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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

New genetic mutations causing hair loss were found in a Chinese family.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

High prolactin levels might be linked to hair loss in autoimmune thyroid disease, but more research is needed.

KRTAP6 genes affect wool quality in sheep.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The Thai version of the Family Dermatology Life Quality Index is a reliable and valid tool for assessing the quality of life of patients' families.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

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

Doctors should set boundaries and seek outside help for family medical issues.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

A new gene mutation linked to a skin condition was found in a Spanish family.

Researchers found a gene mutation responsible for a rare hair loss condition.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The B2 genes are crucial for hair growth in rats.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Baldness is common in Korean men (60.5%), and those with a family history are 3.1 times more likely to have hairline recession.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Hairless gene not strongly linked to baldness.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.