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The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

FGF13 gene changes cause excessive hair growth in a rare condition.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

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

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

A child with a rare vitamin D-resistant condition improved with treatment.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Different body areas in mice produce different hair types due to interactions between skin layers.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Women with PCOS may be more likely to have gum disease than healthy women.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

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

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

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

AFM can diagnose hair disorders by revealing detailed hair surface changes.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

Essential oils from Curcuma species, like turmeric, have compounds that can fight inflammation, cancer, and bacteria, and can also stimulate hair regrowth in bald males.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.