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The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

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.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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

Trichoscopy and trichogram are useful for diagnosing hair and scalp conditions.

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

A 6-year-old girl's inability to grow her hair long was due to Loose Anagen Hair Syndrome, which causes hair to shed easily and may improve with age.

The document concludes that different types of hair loss have specific treatments, and early diagnosis is crucial for preventing permanent hair loss.

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

The document explains various skin conditions and their treatments.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

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.

The document provides a method to classify human hair growth stages using a model with human scalp on mice, aiming to standardize hair research.

Cathepsin L is essential for normal hair growth and development.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

Understanding hair structure and growth is key for diagnosing hair diseases accurately.

Runx1 affects hair growth, cancer development, and autoimmune diseases in epithelial tissues.

Growing hairs are easier to pull out than resting hairs due to different anchorage strengths.

Minoxidil treatment increased hair density in a young Asian girl with short anagen syndrome, but didn't improve hair length or thickness.

A woman's hair loss was due to trichotillomania, which is often misdiagnosed and can require different treatments based on age and underlying conditions.

A blood pressure drug, diltiazem, may also help treat influenza.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Skin and hair changes in horses can indicate serious diseases, and recognizing these signs is important for treatment and management.