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A woman with a rare ovarian tumor and hyperparathyroidism improved after surgery, highlighting the need for reporting unusual cases to understand and manage rare diseases.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Endocrine diseases in dogs often cause skin problems, with hypothyroidism and hyperadrenocorticism being common and leading to hair loss and infections.

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

Prostaglandin analogs like Latanoprost might help grow hair on the scalp and body.

Linear lichen planopilaris can affect the trunk, not just the face.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Two new types of eyelid cysts were identified, each with different treatment challenges.

A new mouse model for vitiligo helps study immune responses and potential treatments.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

Methotrexate effectively controls eye inflammation in Japanese patients with non-infectious uveitis but requires careful monitoring for side effects.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

Discontinuing topical minoxidil can resolve headaches and dizziness.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Women with PCOS and hair loss have lower levels of the protein gelsolin in their blood.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

A man with skin and hair symptoms improved partially with specific treatment.

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

Radiation therapy in breast cancer patients changes gene expression related to DNA damage, fibroblast growth, and hair follicle development, which could help improve treatment for radiation-induced fibrosis.