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Long-term oral and topical treatments improved skin condition in a goldendoodle with a genetic disorder.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A boy's hair loss and bone issues improved with specific vitamin D treatment and calcium.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

Immunotherapy with pembrolizumab significantly reduced cancer in a young woman with adrenocortical carcinoma.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A specific gene mutation causes Olmsted syndrome.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Dupilumab may help children with alopecia areata and atopic dermatitis regrow hair.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Alopecia universalis from alemtuzumab in multiple sclerosis can be reversed with specific treatments.

A potential link exists between unexplained hormone deficiency, hair loss, and testicular tumors, suggesting thorough screening is needed.

People with Down syndrome are more likely to have alopecia areata and need regular skin check-ups.

EPDS can cause recurring scalp sores and hair loss if not treated.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

A rare adrenal gland tumor can cause unusual symptoms due to hormone changes.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Hydroxychloroquine showed some potential, but overall, the three drugs had limited success in treating lupus in dogs.

The 6-year-old Somalian girl fully recovered from her symptoms after successful surgery and treatment.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Zinc supplements effectively treat inherited zinc deficiency in infants.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.