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A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A gene mutation in Lama3 is linked to a common type of hair loss.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

Toe Tourniquet Syndrome is often misdiagnosed.

A misdiagnosed case of HAIR-AN syndrome led to unnecessary surgeries and highlighted the importance of correct diagnosis and treatment.

Men over 50 may experience hormone decline causing various symptoms, and proper management is crucial.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Seven patients were misdiagnosed with discoid lupus instead of lichen planopilaris due to similar symptoms, showing the need for careful diagnosis in scarring hair loss conditions.

Doctors often diagnose Cushing's syndrome late, which worsens symptoms; earlier detection is needed.

The document concludes that accurate diagnosis of alopecia in children relies on thorough examination and history, and while treatments exist, none can alter the course of alopecia areata, which can significantly affect a child's psychological well-being.

The document concludes that with limited resources, the government should focus on impactful enforcement against misleading advertising and encourage businesses to follow guidelines to prevent deception.

Taking biotin supplements can cause incorrect thyroid test results, leading to wrong diagnoses.

Early diagnosis of hair tourniquet syndrome saved a baby's toe from being lost.

The document concludes that early diagnosis of Balint's syndrome is crucial for effective treatment and that understanding drug interactions, like between ritonavir and statins, is important for patient care.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

Better training and awareness are needed to properly diagnose and treat tinea favosa in immigrant populations.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

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

The case shows the importance of quick and thorough evaluation of adrenal tumors to prevent rapid disease progression and poor outcomes.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

The document suggests a clinical trial to accurately determine if PRP is an effective treatment for a common type of hair loss in men.

Doctors often miss Hair Tourniquet Syndrome, which can lead to serious damage if not treated quickly.

A drug helped quickly reduce a movement disorder, experts debated the severity of Raynaud phenomenon, and rapid weight loss was linked to temporary hair loss with good recovery.

A woman was misdiagnosed with hair loss for years, but actually had a rare type of alopecia.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Plasmacytoid dendritic cells are a key factor in causing hair loss in alopecia areata and could help differentiate it from other hair loss conditions.

Testosterone therapy is beneficial for women's health and does not cause masculinization or liver damage, and it protects the heart and breasts.