Search

everythinglearnresearchcommunity

for

Search:↓

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Stopping heptaminol medication reversed hair color loss in a patient on dialysis.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

An 8-year-old girl's eyebrow hair loss was linked to atomoxetine for ADHD but grew back after stopping the medication.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Women's hair loss can be due to hormonal changes and various conditions, with treatments focusing on stopping progression and managing symptoms.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

Low-dose oral isotretinoin improved hair loss and facial bumps in patients with a specific type of hair loss.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

A 35-year-old man had patchy hair loss that was actually due to syphilis, not alopecia areata.

A 6-year-old girl with alopecia universalis regrew most of her hair after treatment with simvastatin/ezetimibe, minoxidil, and prednisolone.

A girl with red hair developed hair-pulling and body image disorders after being bullied for her hair color.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Hair transplantation is a surgical procedure to move hair to bald areas, requires good donor hair, and results show in about a year.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Androgens can both increase and decrease hair growth in different parts of the body.

Children with loose anagen hair have easily pluckable hair due to root sheath problems, and it might improve without treatment.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Minoxidil causes excessive hair growth in almost all patients.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Men with Frontal fibrosing alopecia typically lose hair on the front scalp and sometimes on sideburns and upper lip, with treatments showing varied success.

An improved scalp reduction technique reduces the need for hair grafts and has minimal complications.

Hair loss requires customized treatments based on its various causes and types.