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A 15-year-old girl with hypothyroidism had excess hair and skin issues due to blocked hair follicles.

Trichoscopy can help diagnose early congenital syphilis in newborns.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Gentle hair care and some medications can help manage hair shaft disorders, but no specific treatment exists for congenital issues.

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

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

Netherton's syndrome may have a familial link and doesn't always include atopy.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

The condition is likely inherited in an autosomal-dominant pattern.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

A girl had two rare hair conditions that helped understand their overlap.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

It's important to consider genetic hair disorders when diagnosing hair loss.

Two siblings have a rare genetic condition causing curly, coarse hair.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

Syphilis can cause hair loss without other symptoms and should be considered when diagnosing unexplained hair loss.

A 16-year-old girl with gum overgrowth and excessive hair growth had successful gum surgery and healed well.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Recognizing mild or atypical cases of ectodermal dysplasia is crucial for better treatment and future planning.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A specific gene mutation causes complete hair loss without other health issues.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.