Search

everythinglearnresearchcommunity

for

Search:↓

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Dupilumab significantly improved a 5-year-old girl's prurigo nodularis without side effects.

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

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.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

A patient in Portugal with chronic pulmonary histoplasmosis had a complex medical history and environmental exposures.

Early diagnosis and aggressive treatment are crucial for managing SLE-related pancreatitis in children.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

The girl's skin condition is benign but challenging to treat due to its size and location.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Early diagnosis and treatment of TPP can prevent complications.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Actinic prurigo cheilitis can occur in elderly Asians and can be treated with hydrocortisone cream and sun protection.

Pigmented papules on the ear can be a rare skin condition called cutaneous amyloidosis, treatable with topical tretinoin.

Linagliptin may cause hair loss and skin blisters.

A specific gene mutation causes Olmsted syndrome.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

A woman's hair grew back after she stopped taking the Parkinson's disease medication pramipexole.

A man with a rare disease experienced late hair whitening and loss, but hair color returned, suggesting a good outlook.

Biotinidase deficiency can cause vision and walking problems in children and can improve with biotin treatment.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

People with cleft lip and palate often have respiratory problems.

A 7-year-old girl with non-scarring alopecia will have hair follicle transplantation to improve her quality of life.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Early diagnosis of Keratosis pilaris atrophicans faciei can lead to better, personalized treatments.