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

The conclusion is that cerebrovascular diseases can cause seizure-like activity in stroke patients, which can be improved with antiepileptic drugs.

Stromal cells in melanoma promote tumor growth and spread.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A scalp infection by Mycobacterium abscessus can cause hair loss even in healthy individuals and may be misdiagnosed.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Immunological treatment improved both neuropathy and alopecia.

The hamartoma is an abnormal hair growth with limited development in the upper hair follicle.

Lymphoma should be considered in unusual scalp hair loss cases, as treatment can work but may lead to severe complications.

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

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

Dystonia may be part of PAS-4 and linked to immune issues.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

A hidden autoimmune syndrome was found during a shock, showing thyroid, adrenal, and ovarian issues.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

The surrounding tissue plays a crucial role in the growth and spread of skin cancer.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

The growth of the Epstein-Barr virus in the patient's cells was linked to the worsening of her lymphoma.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

Radiation-induced alopecia after angioembolization usually heals on its own and can look like other hair loss types, but patient history helps prevent misdiagnosis.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Biopsy is crucial to correctly diagnose granuloma annulare, which can mimic other conditions like alopecia mucinosa.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

Dermatologists should consider alpha-gal syndrome in patients with unexplained chronic skin issues.