FACOMATOSIS OFTALMOLOGIA PDF

Retinopathy of prematurity as a major cause of severe visual impairment and blindness in children in schools for the blind in Guadalajara city, Mexico. Br J Ophthalmol. Childhood blindness. Epidemiology and characteristics of childhood glaucoma: results from the Dallas Glaucoma Registry.

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Phakomatosis pigmentovascularis PPV is a syndrome characterized by the association of a vascular nevus with a congenital pigmented lesion epidermal nevus, nevus spilus, and dermal melanocytosis. There are different types of PPV according to the pigmentary nevus associated with the vascular malformation.

Patients may present only the cutaneous condition or have systemic manifestations, among them, trauma, neurological and ophthalmological disorders. We report the case of a 1-year-old girl who had congenital glaucoma. On examination, we identified facial paralysis, bilateral ocular melanosis, segmental capillary vascular malformation on the face as on left trunk and extremities, and aberrant Mongolian spots on the upper back, lumbosacral area and buttocks.

Due to clinical manifestation, the diagnosis of PPV was made. The patient was evaluated by Neurology, Traumatology and keeps on with ophthalmological controls.

Complementary studies are important, to rule out extracutaneous manifestations in PPV. Keywords: Capillary vascular malformation; Child; Mongolian spot; Phakomatosis cesioflammea; Phakomatosis pigmentovascularis. This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features! Clipboard, Search History, and several other advanced features are temporarily unavailable. Search: Search. Advanced Clipboard. Create file Cancel.

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Full-text links Cite Favorites. Abstract in English , Spanish. Similar articles Phakomatosis cesioflammea with late-onset glaucoma and acquired nevus spilus-like lesion - 15 years of follow-up. Chiu HH, et al. Int J Dermatol. PMID: Yang Y, et al. Version 2. Medicine Baltimore. Phakomatosis pigmentovascularis type IIb in association with external hydrocephalus. Okunola P, et al. BMJ Case Rep. Phakomatosis pigmentovascularis: Clinical findings in 15 patients and review of the literature.

J Am Acad Dermatol. Epub Nov PMID: Review. Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Al Robaee A, et al. Pediatr Dermatol. Show more similar articles See all similar articles. Publication types Case Reports Actions. MeSH terms Female Actions. Humans Actions.

Infant Actions. Phenotype Actions. Supplementary concepts Phacomatosis pigmentovascularis Actions. Full-text links [x] Sociedad Argentina de Pediatria. Copy Download.

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