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Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

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 skin problems in Indian children are infections and eczemas.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

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

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

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

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 document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Transgender patients need proper skin care, especially when undergoing hormone treatments, to manage issues like acne and hair loss.

K42 and K124 keratins are only found in horse hoof lamellae.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Progress has been made in skin and nerve regeneration, but more research is needed to improve methods and ensure safety.

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

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

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

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Permanent hair loss from cicatricial alopecia is treated by reducing inflammation and managing symptoms, but regrowth in scarred areas is unlikely.

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

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

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

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

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.

Understanding hair follicles through various models can help develop new treatments for hair disorders.