Search

everythinglearnresearchcommunity

for

Search:↓

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

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.

BB4CMU rice bran oil may help treat hair loss and gray hair.

Valproic acid, a common antiepileptic medication, can cause reversible hair loss in patients.

Thyroid hormone imbalances can cause hair loss in alopecia patients.

Cushing's syndrome can cause serious health problems, and early treatment is crucial, but some issues may remain after treatment.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

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

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

Adults should not consume more than 255 micrograms of selenium per day to avoid risk of hair loss and other side effects.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Diabetes often causes various skin problems and complications.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Eating too much or too little vitamin A can cause hair loss.

Some antiseizure medications can cause reversible hair loss, with valproate, lamotrigine, and carbamazepine being the most common.

Early recognition and treatment of atypical alopecia areata in infants are crucial.

A new mouse mutation causes skin and hair defects due to a gene change.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

CO₂ laser treatment is fast and effective for some benign skin tumors with minimal side effects.

YH0618 helps reduce chemotherapy-induced hair loss by targeting specific proteins and pathways.

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

Most patients with telogen effluvium had low iron and vitamin D levels; iron supplements were commonly prescribed.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The document is a detailed medical reference on skin and genetic disorders.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

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

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.