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Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

Understanding skin structure and development helps diagnose and treat skin disorders.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Some hair protein genes evolved early and were adapted for use in hair follicles.

NF-κB is crucial for different stages and types of hair growth in mice.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

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

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Eruptive vellus hair cysts are often missed in diagnoses.

Some vitamins and minerals like vitamin D and iron can help with certain types of hair loss, but more research is needed for others.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

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

The document is a detailed guide on skin conditions and treatments for dermatologists.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.