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The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The patient had paraneoplastic pemphigus without mucosal involvement.

The document concludes that "hot comb alopecia" is now called "central cicatricial centrifugal alopecia" and its causes are complex.

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.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Trichoscopy is good for telling apart tinea capitis and alopecia areata in kids.

A 13-year-old girl's masculine symptoms improved after surgery for a rare adrenal tumor that produced male hormones.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

Primary essential CVG is a rare, benign scalp condition with treatment focusing on symptom management and hygiene.

Eclipta alba can effectively kill worms like the drug Albendazole.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

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

Early diagnosis and effective treatment of kerion Celsi prevent scarring and permanent hair loss.

Accurate diagnosis of granular parakeratosis is crucial for effective treatment and improvement.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Accurate diagnosis of rare pilomatrix carcinoma is crucial for effective treatment.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Tamsulosin increases the risk of floppy iris syndrome during cataract surgery.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

A horse with severe hair loss was diagnosed with alopecia areata and a yeast infection.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Uncombable hair is inherited dominantly with complete penetrance.

Surgery removed ovarian tumors, normalizing testosterone and improving symptoms.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

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

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.