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Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

PCOS affects nearly 25% of female medical and dental students, impacting their academic and social lives.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Acne vulgaris is a common skin condition that can cause low self-esteem and depression, and early treatment is important to prevent scarring.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

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.

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."

The meeting discussed vitamin D3's role in fighting tuberculosis, potential treatments for skin conditions like psoriasis, and hair follicle regeneration as a possible solution for hair loss.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Skin issues can indicate immune system problems.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A new gene mutation causes insulin resistance in a girl and her mother.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

Frontal fibrosing alopecia and ulerythema ophryogenes may be related and can evolve from one to the other.

Diabetic patients often have ingrown nails due to obesity, high blood pressure, past injuries, bad nail trimming, nail fungus, weak foot pulse, and weak knee reflex.

Iron supplements may reverse premature hair graying caused by iron deficiency.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Finasteride solution helps treat hair loss.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.