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Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

Mesothelioma of the tunica vaginalis testis is rare, often high-grade, and has a median survival of about 24 months.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

The conclusion introduces a new way to classify skin cysts using their shape and genetic markers.

MOF controls skin development by regulating genes for mitochondria and cilia.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

Cystic panfolliculoma resembles hair follicle tumors due to specific cell interactions.

Melanin granules can be expelled by exocytosis.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

The document's conclusion cannot be determined from the provided text.

GnRH treatment can reduce breast cancer cell invasion.

Adipose stem cells show common protein changes as they grow, especially involving S100A6.

Meibomian glands are like hair follicles without a hair shaft.

Waldenstrom’s Macroglobulinaemia can mimic multiple myeloma, so accurate diagnosis is crucial.

Tumor cells in calcifying epithelioma of Malherbe resemble hair follicle cells.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

It's important to understand the differences between FMF and PFM in children.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

A gene mutation in mice causes skin defects and early death.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

Accurate diagnosis of pseudolymphomatous folliculitis is crucial to avoid mistaking it for more serious conditions.

Mouse tail skin has different keratinization near hair follicles and scales.