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Intracorneal vacuoles are common in parakeratotic skin diseases in dogs, especially with more parakeratosis.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Uncombable hair is inherited dominantly with complete penetrance.

Lipedematous scalp may be underdiagnosed and doesn't improve with finasteride.

A young woman with severe symptoms of CPAN improved with intensive treatment but needed a leg amputation.

Recognizing both trichostasis spinulosa and eruptive vellus hair cysts together is crucial for accurate diagnosis and treatment.

A man had a rare pigmented nodule on his scalp that developed from birthmarks.

A large scalp tumor was removed from an elderly woman, who was later diagnosed with schizophrenia.

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

Early recognition and evaluation of nevus sebaceus are crucial to detect and manage potential cancerous changes.

Rathke’s cleft cysts can rarely cause Cushing disease, and surgery can improve symptoms.

Brunsting-Perry pemphigoid can cause scarring hair loss and may be underdiagnosed.

Patients may be at risk for deep vein thrombosis.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

A cat in Turkey had Ehlers-Danlos syndrome, showing very stretchy skin and easy bruising.

Peripilar keratin casts are a helpful sign for diagnosing traction alopecia.

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

Many women in Natal, Brazil, have polycystic ovaries according to ultrasound scans.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

A rare pituitary tumor in an 18-year-old male caused hormonal issues and vision loss, requiring surgery and further treatment.

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A rare ear cyst contained hair fragments.