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ectropion/mrzlica

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ČlankiKliničnih preskušanjPatenti
6 rezultatov

Frontal osteomyelitis presenting as upper eyelid ectropion: A cautionary tale.

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Prijava / prijava
Frontal osteomyelitis is a rare clinical entity that can occur as sequelae to frontal sinusitis, head trauma, as a postoperative complication following sinus surgery or due to haematogenous spread. It usually presents with a soft, fluctuant forehead swelling with pain and fever. Cicatricial

Ichthyosis fetalis in a cross-bred lamb.

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Prijava / prijava
BACKGROUND Ichthyosis is a dermatological disease characterized by varying degrees of generalized hyperkeratosis and alopecia. Two congenital forms of ichthyosis are recognized in animals: fetalis (IF) and congenita. The disease occurs rarely in cattle, swine, dogs, chickens and a goat; it has not

Necrotizing fasciitis after cosmetic blepharoplasty.

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Prijava / prijava
OBJECTIVE To report a case of necrotizing fasciitis after cosmetic blepharoplasty. METHODS Case report. A 74-year-old woman with history of type II diabetes mellitus underwent bilateral upper eyelid blepharoplasty. Postoperatively she developed fever, grayish discoloration of the skin, violaceous

Periorbital necrotising fasciitis in infants: Presentation and management of six cases.

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Prijava / prijava
OBJECTIVE To present the clinical features and management of infants presenting with periorbital necrotising fasciitis (NF). METHODS Retrospective case series. RESULTS Six children were studied. The age at presentation was in the range of 5-11 months (median, 8 months). All children presented with
Recently, a number of medications approved for nondermatologic use have proved useful against dermatologic diseases. This article reviews the dermatologic uses and effects of deferasirox, bortezomib, dasatinib, and cyclosporine eye drops. Deferasirox--an oral iron chelator--could be an effective
TGM1 is the most common gene responsible for lamellar ichthyosis. Previous studies have suggested that patients with lamellar ichthyosis carrying two missense mutations in TGM1 show significantly less severe phenotypes than those with at least one truncating mutation in TGM1. Here, we report a
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