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Sudden, unusual hair loss may indicate serious underlying health issues.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

The document talks about hard-to-treat and rare acne types, their connection with other health issues, the importance of correct diagnosis, and the challenges in managing them.

Foam corticosteroid covers as well as traditional forms.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

5-alpha reductase deficiency leads to male sexual development issues and treatments like finasteride help with prostate enlargement and hair loss.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Fat tissue stem cells may help increase hair growth.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

A new mutation in the HR gene causes hair loss in a specific family.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.