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Frontal fibrosing alopecia and ulerythema ophryogenes may be related and can evolve from one to the other.

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

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that correct diagnosis of alopecia types is crucial, scalp biopsies are important, and more research is needed.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

The document concludes that ongoing medical therapy is crucial for preventing hair loss, and surgical options can restore hair, with future treatments for hair loss being promising.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

AKN might be a skin marker for metabolic syndrome.

GLPLS and LPP are variants of lichen planus.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

Hair loss due to scarring can be treated by reducing inflammation, removing scar tissue, and transplanting hair. The Follicular Unit Extraction technique is effective but requires skill and time. Future focus should be on scar-less healing methods.

New treatments for hair loss should target eight main causes and use specific plant compounds and peptides for better results.

Two unusual cases showed that Lichen Planopilaris can look like other skin conditions and need early treatment to protect hair.

Follicular unit hair transplantation is the standard method for natural-looking hair restoration in androgenic alopecia.

The Shen Bai Hair Growing Decoction may help treat hair loss by promoting hair growth and reducing inflammation.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

KFSD causes scarring hair loss and skin roughness, mainly in males.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

The article explains how to diagnose and manage certain types of scarring hair loss.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

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

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.