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

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

LHX2, with other markers, can identify hair placodes in rats.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

The hair defect is due to abnormal inner root sheath keratinization.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

A woman with Fox-Fordyce disease had symptom relief using tretinoin cream.

Skin can become dry and thick in hypothyroidism.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Mutations in the hairless gene cause a rare form of permanent hair loss.

A rare skin condition causes red and dark patches on the face and limbs.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

The cyst had unusual keratin spherules and resembled bone marrow.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.