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Iron supplements may reverse premature graying in iron-deficient individuals; ingrown nails are common in diabetics with certain risk factors; topical finasteride may reduce scalp DHT as effectively as oral finasteride; monilethrix treatment is challenging but some medications can help.

To prevent and treat Hair-thread tourniquet syndrome in infants, keep a close eye on their limbs, manage maternal hair loss, and educate parents and healthcare providers.

Pilomatricomas should be considered to avoid misdiagnosis in children with unusual skin tumors.

People with cleft lip and palate often have respiratory problems.

Scalp injuries and harsh hair care can cause severe hair matting in children.

Local flaps are effective for covering small to large scalp and forehead defects with good cosmetic results.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

Tamsulosin increases the risk of floppy iris syndrome during cataract surgery.

The boy's symptoms improved with thyroid treatment, and he lost weight, but occasional palpitations persisted.

People with certain hair disorders may also have missing permanent teeth.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A 68-year-old woman with benign mucous membrane pemphigoid has eye, mouth, and skin issues, including thick plaques and nail changes.

Early treatment of mixed connective tissue disease is crucial to prevent severe autoimmune conditions.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Frontal fibrosing alopecia can be diagnosed by examining facial areas and treated with specific medications to stop its progression.

Diagnosing and managing children's hair shaft disorders is challenging but essential.

Polycaprolactone gel is effective and safe for treating nasolabial folds.

Most patients with dermatomyositis had skin rash and were treated with prednisolone and hydroxychloroquine.

A preterm baby's toes were saved from damage by quickly removing a thread that was cutting off circulation.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Tinea capitis needs systemic treatment to avoid severe outcomes.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

The triple rotation scalp flap technique successfully reconstructed a man's scalp with natural-looking hair growth and minimal scarring.

A cat lost hair on its back a month after a road accident, despite no initial skin injuries.

The new Mercedes flap variant effectively closed medium-sized scalp defects in a single operation with good cosmetic results and no complications.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.