Results 141 to 150 of about 30,124 (272)
Unilateral nipple hyperkeratosis [PDF]
Shah, Nehal +3 more
openaire +2 more sources
ABSTRACT Papillon–Lefèvre syndrome is a rare autosomal recessive disorder characterized by palmoplantar keratoderma and aggressive periodontitis. We report an 11‐year‐old Nepalese girl presenting with severe periodontal destruction and characteristic cutaneous manifestations. Clinical and radiographic findings established the diagnosis.
Jenisha Bhattarai +3 more
wiley +1 more source
Acrokeratosis Paraneoplastica-like Findings as a Manifestation of Systemic Lupus Erythematosus
Laura Huilaja +3 more
doaj +1 more source
Nitric Oxide Expression In Oral Mucosa Hyperkeratosis Vs. Leukoplakia
OBJECTIVE: The aim of this study was to determine and compare the (NO) Nitric Oxide expression in oral mucosa hyperkeratosis and in oral leukoplakia lesions.
GHERLONE , FELICE ENRICO +7 more
core
Granulomatous Secondary Syphilis: A Clinicopathological Diagnostic Framework From Three Cases
Granulomatous secondary syphilis is a rare clinical and histopathological presentation that may mimic other granulomatous dermatoses. Clinic pathological correlation, appropriate serological testing, and recognition of characteristic histopathological features are essential for accurate diagnosis.
Sandesh Shah +5 more
wiley +1 more source
ABSTRACT Introduction Therapeutic orthoses, such as medical shoes and custom insoles, are used to prevent diabetic foot ulcer (DFU) recurrence. This systematic review with narrative synthesis aimed to evaluate the effectiveness of orthoses in preventing DFU recurrence compared to standard care.
Behnam Amini +2 more
wiley +1 more source
JAK Inhibitors in Psoriatic–Atopic Dermatitis Overlap: A Four‑Case Series
ABSTRACT Overlap between psoriasis and atopic dermatitis (AD) poses diagnostic and therapeutic challenges; monoclonal antibodies targeting a single axis may improve one component while worsening the other [1]. Janus kinase (JAK) inhibitors act pleiotropically and may provide simultaneous control of psoriatic and eczematous inflammation [2].
Eleonora Bongiovanni +6 more
wiley +1 more source
Focal acral hyperkeratosis [PDF]
Kabir, Sardana +2 more
openaire +2 more sources
Early Acitretin Therapy in a Patient With Harlequin Ichthyosis
ABSTRACT Harlequin ichthyosis (HI) is a rare, severe congenital disorder of keratinization caused by pathogenic variants in the ABCA12 gene resulting in thick, hyperkeratotic plates, deep fissures, and characteristic facial and limb abnormalities.
Orasa Sukmark +2 more
wiley +1 more source

