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Skin conditions like seborrheic dermatitis can make it harder to correctly diagnose hair loss because they can cause the oil glands in the skin to shrink.

Toy poodles may develop harmless mineral deposits around hair follicles as they age.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Lichen planopilaris in men often affects the scalp, eyebrows, arms, legs, and beard, with many having family members with hair loss.

Lichen planus pigmentosus is hard to treat and may be more common in North Africa than previously thought.

Adenolipomas may develop from gland entrapment by fat tissue, showing complex and varied forms.

Postmenopausal frontal fibrosing alopecia may be a unique condition linked to postmenopausal changes.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

Pincer nails are rare in lupus patients and may be managed conservatively.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

Lichen planopilaris is rare, mostly affects older women, and is often linked to autoimmune diseases like lupus.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Increased blood vessel growth in lichen planopilaris may signal active disease needing aggressive treatment.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

The interdisciplinary approach improved the quality of life for a Parkinson's patient and eased staff workload.

Woolly hair is a rare genetic condition with no effective treatments.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

A 10-year-old girl with Fox Fordyce disease improved with treatment, suggesting the disease can occur before puberty and might be underdiagnosed in young girls.

The letter suggests that psychiatric issues, not a sleep disorder, were likely the cause of a patient's self-inflicted leg ulcers.

Regular eye exams are important for detecting serious complications in lupus patients.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

Frontal fibrosing alopecia can occur with lichen planus pigmentosus, needing careful diagnosis and treatment.