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Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

A brown shadow seen in dermoscopy is a marker for lichen nitidus.

The boy likely has a fungal infection causing hair loss.

PAON shows skin patterns due to genetic mosaicism.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A woman's hair loss, resembling an autoimmune condition, improved after treatment, but requires ongoing checks due to potential serious associations.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

The woman has a skin condition involving nodules, scars, and hair loss.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.

Monilethrix causes brittle hair and hair loss, and it runs in families.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

The cyst had unusual keratin spherules and resembled bone marrow.

Anti-MND antibodies are present in various diseases, not just PBC, and their levels don't correlate with disease activity or skin symptoms.

A new genetic mutation was found causing hair and eye issues in a boy.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

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

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

Thorough evaluation and treatment are crucial for thyroid nodules.

The scalp has a natural speckled pattern of increased pigment around hair follicles, possibly linked to local hormone production.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Sebaceous nevus changes with age, and dermoscopy and RCM are effective for diagnosis.