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A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Autoimmune and inflammatory processes are involved in both scarring and non-scarring types of hair loss.

Platelet-rich plasma therapy may rarely trigger herpes zoster ophthalmicus.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Three dogs with a rare skin condition improved with treatment.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Lichen planopilaris can unusually affect only the face, causing pigmentation and scarring.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.

Systemic corticosteroids can cause unusual skin issues in people with juvenile rheumatoid arthritis.

A new mouse mutation causes skin and hair defects due to a gene change.

Two rare bald spots on the back of the scalp were found to be lupus, not alopecia areata.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The woman has scurvy and needs more vitamin C.

Digital gangrene can be an initial symptom of late-onset systemic lupus erythematosus.

A rare skin condition usually on the face was found on a man's heel.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

People with Lichen sclerosus are more likely to have skin conditions like vitiligo and alopecia areata, heart disease risks, and other health issues. They should be checked for these, but screening plans shouldn't differ based on gender due to lack of data.

Argentine-cross polo ponies commonly develop sarcoid tumors with distinct types and histopathological features.

Sonidegib often causes hair loss, and LC-OCT helps identify early signs.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

The girl's swelling and skin issues improved with fluid restriction and diuretics.

Sarcoidosis can mimic other skin disorders, making diagnosis challenging.