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Hair loss from Telogen Effluvium can be managed by treating the underlying cause and may improve with treatments like minoxidil.

Hair keratin treatments can be harmful, potentially causing health issues like skin reactions and cancer.

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.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

Activating β-catenin increases melanocytes and decreases Schwann cells.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Neurohormones help control skin health and could treat skin disorders.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

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

Low-level laser therapy effectively reduces the size of pressure ulcers compared to placebo.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Transplant patients often get skin problems, with treatments varying by condition.

The document lists various dermatology topics, treatments, and diagnostic methods.

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 reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The symposium concluded that hair growth involves complex processes, including the hair follicle life cycle, the role of the dermal papilla, hair strength, pigmentation, and the impact of diseases and treatments like minoxidil on hair and skin.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

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

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Monilethrix causes different levels of hair loss in family members.

Merkel cells and Langerhans cells in hair follicles are closely connected and may interact.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Eruptive vellus hair cysts are often missed in diagnoses.

Skin changes during pregnancy are common, and non-invasive imaging is safe for monitoring these changes.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.