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The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Lichen planopilaris can occur with multiple autoimmune diseases.

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

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Sarcoptes scabiei infection causes significant health and behavior changes in wombats.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.

The dog's skin and anemia issues returned after stopping treatment for Babesia gibsoni.

Werner's syndrome causes early aging and increases cancer risk, requiring early diagnosis and symptom management.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Most hair loss in captive rhesus macaques is likely due to environmental and behavioral factors.

A woman with type 2 diabetes developed alopecia areata, suggesting a link between the two autoimmune conditions.

Consider Castleman's disease in similar cases; histology and steroids help diagnose and manage it.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Adrenomyeloneuropathy (AMN) can cause bladder problems due to nerve damage.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A goat had skin issues caused by Malassezia slooffiae, marking the first known case in goats.

Mutations in the LIPH gene cause woolly hair in a child.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

Dogs have a skin condition like human pseudopelade, causing hair loss that doesn't improve with treatment.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

Trichoblastomas in aged house musk shrews show unique features and may involve serum amyloid A in inflammation.