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The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

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

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

EZH2 levels decrease as fetuses develop and are higher in adult skin, which may affect skin growth and repair.

Hormone treatment caused hair loss, finasteride helped regrowth.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

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.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

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

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

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

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

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

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Oral minipulse therapy effectively treated bullous lichen planus in a 35-year-old woman.

Dr. SKS hair booster serum effectively treats hair loss caused by COVID-19.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

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

There have been major advances in diagnosing and treating hair loss over the last 30 years, with new drugs and improved hair transplant techniques.

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.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Biotin supplements significantly improved a young girl's uncombable hair.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

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

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