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COVID-19 can cause hair and nail disorders after infection.

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

The document's conclusion cannot be provided because the text is not in a processable format.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.

Pili anulati may cause hair loss, proper diagnosis and treatment needed.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Some families have a genetic condition where they are born with irregular scalp defects.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

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

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The man had myotonia, which caused delayed hand grip relaxation.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

A specific gene mutation causes sparse, brittle hair in a family.

A baby boy's toe was saved from damage caused by hair strangulation by quick surgical treatment.

Hair casts, also called pseudonits, are often mistaken for other conditions.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

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

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

Trichothiodystrophy causes unusual hair and developmental issues.

A Korean girl developed kinky hair without known cause or effective treatment.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Defective mink guard hairs have split tips and missing cuticle cells, causing a metallic sheen.