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A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

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

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

A toddler with a rash and developmental delays improved after treatment for severe malnutrition caused by a diet lacking in protein.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

A man with vitiligo and alopecia saw quick skin and hair improvement with ruxolitinib, but skin color gains were lost after stopping treatment.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

The boy's hair and skin color differences are due to a pigmentation disorder.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Rituximab treatment led to complete hair regrowth and improved skin in a woman with pemphigus foliaceus.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Platelet-rich plasma might be a new way to treat lichen planopilaris.

The new treatment improved keratosis pilaris symptoms and mood in 28 days.

Increased blood vessel growth in lichen planopilaris may signal active disease needing aggressive treatment.

Salicylic acid ointment effectively treated a toddler's skin condition.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

There's a red birthmark on the scalp.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Pseudofolliculitis causes painful bumps and dark spots from shaving, especially in people with curly hair, and can be treated by changing shaving habits and using specific topical treatments.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

Pentoxifylline effectively improves pretibial pruritic papular dermatitis.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.