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The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Early treatment of acne is crucial to prevent scarring and psychological effects.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

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

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

A 2-year-old girl had a hair disorder not shared by her identical twin.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Woolly hair is a rare genetic condition with no effective treatments.

Monilethrix causes fragile, patchy hair loss.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Most patients with hair loss sought treatment for cosmetic reasons, were unhappy about their appearance, and had a family history of the condition, suggesting it may be inherited.

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

Monilethrix causes different levels of hair loss in family members.