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The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.

TGM3 is important for skin and hair structure and may help diagnose cancer.

A new mouse model for vitiligo helps study immune responses and potential treatments.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Isotretinoin can effectively reduce symptoms of frontal fibrosing alopecia.

Female pattern hair loss in Western India is common and often linked to metabolic syndrome.

Gonadal hormones significantly affect the severity of alopecia areata in mice.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman showed neurological symptoms from psittacosis linked to bird exposure, improving after antibiotic treatment.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Choose hair restoration surgery candidates carefully and plan treatments for a natural look and future hair loss.