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FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

The dog likely has a condition similar to Canine alopecia X.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

Syphilis can cause unexpected symptoms like hair loss in well-managed HIV patients, so doctors should stay alert.

Trichodysplasia spinulosa is a rare skin condition linked to weakened immune systems, mostly in organ transplant patients.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Sorafenib often causes mucositis, hand-foot syndrome, rash, alopecia, diarrhea, and fatigue.

The man likely has secondary syphilis affecting his nervous system.

A woman with lupus had blood cell destruction, treated successfully with medication.

Sickle cell anemia causes hormone issues and delayed puberty due to testicular failure.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Syphilis can cause hair loss in some cases.

Syphilis can cause hair loss without other symptoms and should be considered when diagnosing unexplained hair loss.

Rapunzel syndrome is more common in Asian countries and requires early diagnosis, especially in Asian girls.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Most people with metabolic syndrome in Brazil have skin issues, especially if they are morbidly obese.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

Sarcoidosis is more common and severe in Black patients than in Caucasians, requiring early diagnosis and treatment.

A 38-year-old African American woman has a rare condition that prevents her from growing long hair.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The boy's scurvy symptoms improved with vitamin C treatment, highlighting the need for a balanced diet.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.