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

Iron deficiency can cause hair loss and often signals underlying health issues.

Androgenetic alopecia is a long-term, immune-related disorder that starts during puberty due to androgen secretion, and it might be improved with iron tablets, platelet transfusion, and anti-inflammation therapy.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

The boy's hair and skin color differences are due to a pigmentation disorder.

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

Children's hair needs only a little iron for normal growth, regardless of their body's iron levels.

Reticulocyte hemoglobin content is the best indicator of iron deficiency in women with diffuse non-scarring hair loss.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

LIPH mutations cause woolly hair in some Chinese people.

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

A woman with Budd-Chiari syndrome improved after treatment and needs a liver transplant, highlighting the importance of considering non-criteria antiphospholipid syndrome in similar cases.

A man's skin condition and poor diet led to a scurvy diagnosis.

CDH3-related disease causes worsening eye and hair issues.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Two new gene mutations cause a rare hair disorder.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Mutations in the hairless gene cause a rare form of permanent hair loss.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Parental socioeconomic status doesn't improve dietary habits or reduce disease severity in children with sickle cell disease.

Early iron deficiency can lead to anemia during puberty, so it's important to address it early.

Specific keratin gene mutations can cause monilethrix.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.