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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The document informed plastic surgeons about upcoming educational events worldwide.

Upcoming events and courses in plastic surgery were announced.

El acetato de ciproterona trata problemas androgénicos como hirsutismo, acné, seborrea y alopecia con diferentes dosis y combinaciones.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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

A new system helps better diagnose and treat female androgenization conditions like PCOS.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

The Free Androgen Index is important for diagnosing PCOS due to its strong link with symptoms and risk factors.

The French Endocrine Society suggests diagnosing PCOS with two of three signs, recommends lifestyle changes and clomiphene for treatment, and calls for more research on certain treatments and tests.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

FGF5 gene mutations cause long hair in domestic cats.

Hair bands are a new symptom of facio-genito-popliteal syndrome.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

PRIDE syndrome includes skin and hair issues from cancer treatment with EGFR inhibitors.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Trichoscopy helps diagnose frontal fibrosing alopecia in Caucasians, but more research is needed.

Recognizing rare hair loss patterns in young females can improve understanding and treatment.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Men with Frontal fibrosing alopecia typically lose hair on the front scalp and sometimes on sideburns and upper lip, with treatments showing varied success.

A 6-year-old boy in India was diagnosed with Bloom's syndrome, showing growth and developmental issues, and skin problems worsened by sunlight.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Frontal fibrosing alopecia has occurred in two related male families.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.