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Genetic factors and diet significantly increase the risk of male pattern baldness.

Understanding and treating alopecia areata improves patient care.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Platelet-derived bio-products help in wound healing and tissue regeneration but lack standardized methods, and their use in medicine is growing.

A specific gene variant may increase the risk of developing Alopecia Areata.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Skin reactions are a common reason for emergency visits due to drug allergies, with some severe cases needing intensive care.

Two gene variants cause white spots in cattle.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

New vitiligo treatments focus on controlling immune damage and restoring skin color.

Steroid 5α-reductase evolved from protists and diversified in eukaryotes, with specific roles in mammals and plants.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The document concludes that "hot comb alopecia" is now called "central cicatricial centrifugal alopecia" and its causes are complex.

The new SLICC criteria for diagnosing lupus are more sensitive and accurate than the old criteria.

Alopecia areata and vitiligo can coexist, respond well to treatment, and may have a better prognosis together.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

COVID-19 and vaccines cause various skin reactions and highlight the need for dermatologists in managing these issues and addressing vaccine distribution disparities.

Ophiasis mainly affects females, lasts longer, and has lower regrowth rates, with a new classification system helping predict treatment response.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

Certain genes influence the direction of hair whorls on the scalp.

New digital tools are improving the diagnosis and understanding of irreversible hair loss conditions.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Some women with PCOS have rare genetic variants linked to the condition.