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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Alopecia can be caused by multicentric reticulohistiocytosis.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Daughters with affected mothers may develop frontal fibrosing alopecia early.

The guideline offers recommendations for diagnosing and managing PCOS and its complications.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Many genetic syndromes are linked to alopecia areata in children, but most are rare and not fully understood.

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

Physical activity, height, and smoking affect prostate cancer risk.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The condition might be caused by genetic changes after birth.

People with celiac disease have a higher risk of developing alopecia areata.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Asthma may increase the risk of alopecia areata.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

New genes linked to male pattern baldness were found on chromosome 20p11.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

New genetic locations explain much of hair color variation in Europeans.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.