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Skin biopsy is crucial for diagnosing unknown baldness causes.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Most orthodontic patients with missing teeth also have hair disorders.

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.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Red and infrared light therapy improves hair growth in balding patients.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

Msx2 and Foxn1 are both crucial for hair growth and health.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

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."

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.