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Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

A woman had severe reactions to methotrexate, including skin issues and organ problems, but improved after 38 days in the hospital.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Methimazole can cause severe low platelet count in Graves' disease patients, so monitoring and alternative treatments are important.

Deleting MED1 in skin cells causes hair loss and skin changes.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Low-dose methotrexate is generally safe but can cause mild to severe side effects, and folic acid can reduce these risks.

Doctors need to recognize and treat metabolic disorders in children early to prevent serious health issues.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

High-dose methotrexate can cause severe skin and nail issues.

Monilethrix is a rare genetic hair disorder that's hard to treat.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Some children with methylmalonic and propionic acidaemias have skin problems related to their condition and diet.

Genetic disorders can disrupt mineral and trace element metabolism, affecting health.

Certain amino acid analogues can inhibit wool and hair growth and affect fiber strength.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

A unique gene mutation was found in a family with monilethrix.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

Mutations in the HOXC13 gene cause hair and nail development issues.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

Melanin may help melanoma cells grow by aiding their metabolism.