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The condition might be caused by genetic changes after birth.

The patient's long-term symptoms were due to Sheehan's syndrome, which improved with hormone therapy.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Excessive body hair can signal complex health issues.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Trichoblastic carcinoma may be a distinct type of skin cancer different from basal cell carcinoma.

Diagnosing PCOS in teenagers is hard because its symptoms often look like normal puberty, and there's a need for better diagnosis methods and agreement on criteria.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Acneiform follicular mucinosis can be controlled with systemic corticosteroids.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.

Topical treatments helped a child with Down syndrome and severe hair loss regrow most of his hair.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

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.

A rare ovarian tumor caused a postmenopausal woman to develop male-like features, which improved after surgery.

Genetic testing for EGFR mutations is crucial in similar cases.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Six genetic conditions are often linked to complete scalp hair loss in children.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

Early diagnosis and multidisciplinary care are crucial for managing PCOS in adolescents.

Male pattern hair loss is diagnosed and treated earlier and is milder, possibly due to early puberty.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Ossification in trichilemmal cysts is more common than previously believed.

A woman with anorexia and Cushing's syndrome improved after tumor removal, highlighting the need to consider hormonal issues in psychiatric conditions.

People with polycystic ovary syndrome have worse meibomian gland and ocular surface conditions.