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Caffeine may help hair growth in hereditary hair loss.

Hair damage shows as fragility, dullness, and discoloration, varies by ethnicity, and is worsened by cosmetic procedures and diseases.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Using the right hair care products can improve hair health and help manage hair disorders.

Hair transplantation successfully treated a woman's hair loss caused by a tight ponytail.

The document says that there are treatments for hair and nail diseases.

A patient experienced long-lasting hair loss after using acitretin for psoriasis.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

The document concludes that different types of hair loss have specific treatments, and early diagnosis is crucial for preventing permanent hair loss.

Hair loss in children is often caused by scalp infections, immune disorders, hair pulling, stress, and requires careful treatment due to emotional effects.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

Hair loss in young adults is common and varies in pattern, cause, and type.

Hair changes can indicate systemic diseases or medication effects.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

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

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

Genetic testing is crucial for diagnosing rare hair loss disorders.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Women with diffuse hair loss often have lower iron and vitamin D levels, but their thyroid function is typically normal.

Trichoscopy is a useful tool for diagnosing hair and scalp diseases without needing skin biopsies.

The document concludes that accurate diagnosis of hair disorders is crucial and requires a range of diagnostic methods.

Hair can indicate early signs of metabolic disorders, with issues like protein deficiency stopping hair growth.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.