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Some blood donors on teratogenic drugs may have unsafe drug levels, suggesting a need for better deferral policies.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

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.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Human Beta Defensin 1 levels do not predict the risk or severity of Alopecia Areata.

Higher NLR, PLR, and MPV may help diagnose androgenetic alopecia.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Children with frequent severe infections and low antibodies should be checked for immune deficiencies.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Multiple platelet donations do not affect blood cells and plasma proteins in donors.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Many young women who donate blood have hormonal disorders like excess male hormones and PCOS.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Hair root sheaths can be used to accurately analyze genetic markers.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new method accurately determines hair blood type and can be used on dust samples.

The study found that the quality of cord blood units remains consistent before freezing and after thawing, indicating that attached tube segments reliably represent the graft's properties.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Machine learning can use blood tests to help predict moderate-to-severe alopecia areata.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

Iron supplements helped female blood donors with low iron avoid anaemia and return to donate again.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Higher RBP4 levels found in people with two types of hair loss.

A simple test can help diagnose a rare bruising disorder after ruling out other causes.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Blood cell counts could help predict and treat alopecia areata and telogen effluvium.

Dermatologists should be involved in the care of hematology patients due to common skin issues.