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A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

Reduced Sonic hedgehog signaling leads to increased HPV replication and wart formation.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Blood tests confirmed a baby in the womb had a CMV infection.

Thermography matched the patient's pain levels in a shingles case and might help diagnose shingles without a rash.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

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

A man had two rare autoimmune diseases that might be connected.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Twins had rare skin cysts likely due to genetics.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A new mutation in mice causes crooked whiskers and messy hair.

A patient with pemphigus vulgaris improved significantly after treatment for an additional viral skin infection.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

The woman was diagnosed with Vogt–Koyanagi–Harada disease and successfully treated with medication, restoring her vision and stopping headaches.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

A gene mutation in mice causes permanent hair loss and skin issues.

Viral reactivation is rare at the time of DRESS diagnosis in the U.S.