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Early recognition and treatment of severe SLE symptoms can improve outcomes.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Feeding steers only Leucaena leucocephala causes severe health issues and poor weight gain.

Woman with diabetes had hair loss due to rare ovarian tumor; surgery improved hair growth.

Early minipulse corticosteroid therapy can effectively treat scalp discoid lupus in children.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Monilethrix causes different levels of hair loss in family members.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

A patient with a rare form of lupus improved after treatment for skin ulcers and hair loss on the face and scalp.

The boy's hair fully regrew after treatment for a rare hair loss condition.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

A new mutation in the HR gene causes hair loss in a specific family.

A three-year-old girl survived a rare serious infection caused by BCG vaccination, which improved after treatment with a leprosy drug.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

Most lupus patients in coastal Kerala had skin-specific lesions that could help diagnose the disease, and non-specific skin issues were linked to more severe, systemic lupus.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.

The twins' condition is unique and doesn't match any known syndromes.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.