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A new skin disease in four Labrador retrievers responded well to immunosuppressive treatment.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

A girl had rickets due to a gene mutation affecting vitamin D response.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

FGF5 gene mutations cause long hair in domestic cats.

Skin changes help detect graft-versus-host reaction early after bone marrow transplants.

A man with Isaac's syndrome affecting only one side of his body improved after immune system-targeted treatment.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.

IVIG therapy was linked to hair regrowth in two patients with hair loss, but it's not recommended due to its risks and costs.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Glutamic acid helps increase hair growth in mice.

Chronic T. gondii infection may harm male fertility.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

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

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

A gluten-free diet improves growth and reduces symptoms in children with celiac disease.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Genetic factors influence growth and brain development in children.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Gefitinib can cause scalp skin issues and permanent hair loss.