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Trichoscopy helps accurately diagnose temporal triangular alopecia.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

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

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

A rare ovarian tumor caused a postmenopausal woman to develop male-like features, which improved after surgery.

Follicular mucinosis in a 15-year-old is usually harmless but needs monitoring for possible lymphoma.

Tofacitinib successfully treated a woman's severe symptoms from a rare autoimmune condition.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

Mitochondriopathy may cause eyelash loss.

Long-term use of minoxidil may cause hair follicles to transform into noticeable terminal hairs, leading to trichostasis spinulosa.

An 8-year-old boy with bed-wetting issues suffered a severe penile injury from tying a thread around his penis, requiring urgent medical treatment to avoid worse outcomes.

Temporal triangular alopecia usually starts in early childhood and treatment with Minoxidil has limited effectiveness.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

TB lymphadenitis can occur in people with weakened immune systems, like those with SLE.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

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

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

People with polycystic ovary syndrome have a higher chance of having chronic thyroiditis.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

Early referral to a pediatric rheumatologist and thorough evaluation are crucial for treating complex overlap syndromes effectively.