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A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

Fibrosing alopecia in a pattern distribution is a new type of scarring hair loss that resembles common baldness and an autoimmune skin disease.

Always consider xanthomatous hypophysitis before deciding on pituitary surgery.

Certain types of mucopolysaccharidoses cause significant hair abnormalities.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Hormonal therapy is essential in late-diagnosed Kallmann's syndrome to prevent bone issues.

Different PCOS subgroups have similar metabolic features, but those without menstrual problems have milder issues.

A new gene mutation causes a rare type of hair loss.

Polycystic Ovary Syndrome (PCOS) is a common but often undiagnosed disorder in women that can cause irregular periods, infertility, and other symptoms, and can be managed with lifestyle changes, medication, and sometimes surgery.

The boy likely has a fungal infection causing hair loss.

PCOS requires comprehensive, lifelong care addressing both visible and hidden health issues.

Women with PCOS often feel anxious and distressed about their appearance, especially in social situations.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Polycystic ovary syndrome is a common hormonal disorder in women that affects health and fertility.

Hair loss improved after removing pituitary tumor.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

KID syndrome should be reclassified as an ectodermal dysplasia.

Androgenetic alopecia in teens is linked to obesity and other metabolic risks, needing early diagnosis and management.

Body dysmorphia is common in women with PCOS, affecting their quality of life.

Early diagnosis of pseudopelade of Brocq in men is crucial to prevent permanent hair loss.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A 16-year-old girl with gum overgrowth and excessive hair growth had successful gum surgery and healed well.

Steroid pulse therapy improved symptoms in a man with Satoyoshi syndrome.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

The conclusion is that more women in their forties are getting AGA and stress is linked to AGA in both men and women.