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A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Clinical signs of excess male hormones and actual hormone levels in the blood do not always match in women with polycystic ovary syndrome.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Besnoitiosis, a parasitic disease, has been found in donkeys in Italy and may be more common in Europe than previously thought.

Psoriasis patients on biologic therapy have a weaker immune response to COVID-19 vaccination than healthy people.

People with vitiligo may have a lower risk of heart disease.

RDW can be a useful marker for inflammation in alopecia areata patients.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

The boy's symptoms suggest a possible new medical condition.

Valproic acid may cause hair loss by reducing biotinidase enzyme activity in rats.

Women with early hair loss have higher blood pressure and aldosterone; screening and treatment may help.

Alopecia areata severity and symptoms vary by race and ethnicity.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Male pattern baldness is linked to higher levels of a certain receptor in the scalp, which leads to the shrinking of blood vessels and hair loss. Early treatment targeting this receptor could be more effective.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Alopecia areata patients have a higher risk of blood clots.

Men with male pattern baldness are more likely to have unhealthy blood lipid levels, which could signal other health issues.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

People with Alopecia Areata and Androgenic Alopecia have more mast cells in their scalp than healthy individuals, especially those with Alopecia Areata.

HIV-positive men who have sex with men have a higher rate of anal beta-papillomavirus infections.

The conclusion is that the hair loss in the patients was likely due to alopecia areata, not boron exposure.

PRP injections improve hair thickness for baldness.

Selenium levels are similar in healthy people from both high and low NPC risk areas.