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Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

People with migraines often have mental health conditions, and treatment should be personalized to address both issues safely.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

A Japanese man with rare skin conditions improved with hydroxychloroquine treatment.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

The document explains different hair and scalp conditions, including common hair loss after pregnancy or illness, drug-induced hair loss, hereditary excessive hair growth, patterned baldness, autoimmune hair loss, and permanent loss due to skin disease, with generally limited treatment options.

Alopecia areata is a hair loss condition caused by immune factors and can be treated with JAK inhibitors.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

A 5-year-old Akita with a rare skin condition improved significantly after treatment.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Alopecia areata is a hair loss condition that may be linked to stress and genetics, often requires psychological support, and has no set treatment.

The conclusion is that managing hair loss conditions like FFA and melanoma requires individualized approaches, considering new findings and balancing treatment benefits with potential risks.

Acne keloidalis nuchae is a chronic skin condition more common in African men, causing itchy or painful bumps and can lead to permanent hair loss if not treated early.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A patient with a rare chromosome condition also had a rare type of hair loss.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The document is a detailed medical reference on skin and genetic disorders.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Obesity increases the risk of skin infections, inflammatory conditions, and melanoma, but not basal cell carcinoma.

The book explains how excess male hormones can affect various conditions like Polycystic Ovary Syndrome and Cushing's disease.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Polycystic Ovary Syndrome (PCOS) in teenagers is a complex condition linked to genetics and environment, often associated with obesity and insulin resistance, and is treated with lifestyle changes and medication.