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A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Removing keratin plugs and ingrown hairs improved scalp inflammation.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

New findings on hair keratin, wound healing, and skin blistering were presented.

Certain genetic variants in keratins increase the risk of tooth decay.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Keratin biomaterials from human hair help nerve regeneration by activating Schwann cells.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Feathers become harder as they develop due to a change in keratin type.

Schimmelpenning Syndrome requires careful evaluation and tailored treatment for skin, eye, and developmental issues.

The document found differences in lesion distribution and microscopic features among trichostasis spinulosa and similar skin conditions.

Cornification is the process where living skin cells die to create a protective barrier, and problems with it can cause skin diseases.

Prompt treatment of inflammatory tinea capitis (kerion) is crucial to prevent scarring and hair loss.

PC-associated alopecia has unique microscopic features.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

A young athlete's fragile hair condition improved by cutting hair and using gentle shampoo.

Specific keratin gene mutations can cause monilethrix.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.