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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A woman with severe hair loss due to systemic sclerosis regrew her hair in 4 months using a combination of treatments.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

A rare ovarian tumor in a 2-year-old girl was successfully removed, normalizing her hormone levels.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Acneiform follicular mucinosis can be controlled with systemic corticosteroids.

Trichobezoars can cause serious health issues like biliary obstruction, and treatment includes surgery and therapy to prevent recurrence.

Ovarian hyperthecosis can cause high testosterone and symptoms like hair loss, and surgery can help improve these symptoms.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Long-COVID can cause lasting symptoms, but treatment with Erbisol drugs may help.

PFS might be a delusional disorder with potential to become mass psychogenic illness.

A special blood test helped find the overactive ovary in a teen with PCOS, and removing that ovary improved her condition.

PCOS causes hormonal imbalances, irregular periods, and can lead to infertility, obesity, and mental health issues.

Negative illness perceptions increase emotional distress, worsening OCD symptoms in alopecia areata patients.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Lichen planopilaris can occur with multiple autoimmune diseases.

A young woman had a rare, aggressive ovarian tumor that was hard to diagnose and treat, leading to disease progression despite treatment.

A patient with Ehlers-Danlos Syndrome improved after treatment for fat malabsorption and essential fatty acid deficiency.

An isolated episcleral plasmacytoma can mimic episcleritis, making diagnosis challenging.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

The type of PCOS a woman has doesn't strongly predict her skin or metabolic symptoms; obesity is a more important factor.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Alopecia areata and myasthenia gravis can occur as rare symptoms of breast cancer.

Loose anagen hair syndrome causes easily pulled, thin hair in kids but is harmless and temporary.

Traumatic anserine folliculosis is a harmless skin condition in young males that needs correct diagnosis to avoid unnecessary treatments.

Steroid cell tumors in the ovary are rare, can produce testosterone causing symptoms, and are mainly treated with surgery.