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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Soft-tissue calcification is rare in systemic lupus erythematosus.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition that may respond to antiandrogen therapy.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Areata-like lupus can mimic alopecia areata but is a form of cutaneous lupus erythematosus.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Women with lichen planopilaris and frontal fibrosing alopecia often have other health issues like hypothyroidism and lupus.

Frontal fibrosing alopecia can sometimes look like syphilitic hair loss.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Protein-losing enteropathy worsened with lupus symptoms but improved with prednisolone.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

Early detection and treatment of primary biliary cirrhosis and related autoimmune diseases improve outcomes.

Repeated biopsies are crucial for managing lupus panniculitis when initial treatments fail.

A boy had a rare scalp condition with thickened skin and different-colored hair.

Finasteride reduces movement issues in Parkinson's disease rats.

Different types of female pattern hair loss have unique characteristics and are associated with various health conditions.

A rare form of lupus can cause severe nerve damage and other symptoms, but treatment can help.

Giant axonal neuropathy changes the structure of keratin in human hair.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

A 20-year-old had hair loss and skin issues from lichen planopilaris starting at age 10.

A woman's hair loss was misdiagnosed as alopecia areata but was actually lichen planopilaris, needing immediate and ongoing treatment.

A new form of lipodystrophy in HIV patients causes neck fat buildup.

A 42-year-old woman had a scalp lesion that didn't cause hair loss and showed specific changes under a microscope.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Physical symptoms in depression can reveal underlying medical conditions.