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Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

Certain genes control the color of human hair by affecting pigment production.

The skin lesion was diagnosed as a matrical cyst with unusual features.

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

Pregnancy with Cushing's syndrome is rare and risky for both mother and baby, needing early diagnosis and treatment.

Melanocyte progenitor cells are found in human fat tissue and can become mature melanocytes, which may help treat skin issues.

EF and PXE not closely related.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Pituitary imaging is recommended for hyperprolactinemia due to common pituitary issues.

A 50-year-old woman with breast cancer developed an autoimmune skin disorder, highlighting the need for thorough checks and team-based treatment.

ECCL should be considered in patients with specific skin and eye lesions.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Histopathological examination is crucial to avoid misdiagnosis and ensure proper treatment for skin lesions.

Botulinum toxin A effectively treated a man's facial cysts with no side effects and lasting results.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Onycholemmal horn is a rare nail tumor in elderly women, treated by surgical removal.

Selenium levels are similar in healthy people from both high and low NPC risk areas.

First-episode psychosis patients have higher hair cortisol levels, indicating early stress response issues.

A mare had a functional ovary with a tumor containing cartilage and bone.

Normal androgen levels need ACTH, and different mechanisms control adrenarche and gonadarche.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

CK 5/6 expression in breast cancer is linked to negative hormone receptor status and higher tumor grade.

Korean patients with PCOS often have skin problems like acne and excess hair, with different symptoms based on their specific PCOS type.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

EPI-NCSCs from hair follicles may help treat brain development issues in mice.

Scalp melanomas are more dangerous and often missed, needing earlier detection.