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Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

A cat had a rare skin disorder with hair loss and scaling, linked to a suspected tumor.

LIPH mutations cause woolly hair in some Chinese people.

The dog likely has a condition similar to Canine alopecia X.

A 16-year-old girl with lupus symptoms improved with treatment despite negative ANA tests.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

A rare skin condition was found in a Labrador retriever outside North America.

Satoyoshi syndrome can occur without causing premature ovarian failure.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A rare skin condition causes red, dark, bumpy facial lesions.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Tislelizumab can cause cutaneous lupus erythematosus.

A specific gene mutation causes Olmsted syndrome.

A young woman with severe symptoms was diagnosed with SLE and improved significantly after treatment.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

A woman with Sheehan syndrome improved with hormone treatment.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

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.

A dog in Colorado was diagnosed with leishmaniasis, suggesting the disease might be present in the state.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

Generalized hair follicle hamartoma can occur with systemic lupus erythematosus.

Correct diagnosis and treatment of lupus vasculitis improved the woman's severe symptoms.

Early diagnosis and treatment of myositis in SLE patients lead to positive outcomes.

Follicular mycosis fungoides can look like a B-cell lymphoma, making diagnosis difficult.