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People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

A woman was diagnosed with a rare adrenal gland cancer that did not show usual hormone-related symptoms.

Onychomatricoma is a unique nail tumor, not related to other hair-related tumors.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

Vismodegib can cause muscle spasms, taste changes, hair loss, fatigue, weight loss, and possibly new issues like skin cancer, dehydration, and swallowing problems, needing close monitoring.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

A rare hair follicle tumor in the hand was successfully removed with no return after four years.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

Rabbits with mange recovered after ivermectin treatment.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

A girl with Rapunzel syndrome had surgery to remove a hairball, and addressing mental health is important to prevent it from happening again.

Keratoacanthomas and squamous cell carcinomas have similar keratin patterns, making them hard to tell apart.

Vitamin D supplements should be used cautiously in sarcoidosis patients, with regular monitoring to avoid high calcium levels.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

Melanocyte stem cells can become melanoma, resembling human melanoma.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

Spontaneous keloids may be linked to nephrogenic systemic fibrosis in dialysis patients.

The LMNA mutation affects skin structure even in asymptomatic carriers.

The nodule on the woman's back was a benign hair follicle tumor, not cancer, but needed removal.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.