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A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Frontal Fibrosing Alopecia is a slowly progressing hair loss condition, likely underdiagnosed, with ineffective treatments, needing more research to understand it fully.

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Microinflammation is more intense in smaller hair follicles and may be linked to hair loss.

Inclisiran is effective at lowering cholesterol.

Some families have a genetic condition where they are born with irregular scalp defects.

Combining Ficlatuzumab and Gefitinib can cause severe hair loss.

Snail1 may contribute to fibrosis in frontal fibrosing alopecia in postmenopausal women.

Frontal fibrosing alopecia is a scarring hair loss condition mainly affecting postmenopausal women, with unclear causes.