Aspectos clínicos e manejo terapêutico da Anomalia de Peters: um relato de caso
نویسندگان
چکیده
A Anomalia de Peters é uma malformação do segmento anterior olho, secundária a um defeito na migração das células da crista neural. É caracterizada por opacidade corneana central e alterações no estroma posterior, membrana Descemet endotélio. O objetivo deste artigo ilustrar tipo I, relatando caso paciente 4 anos, assim como discutir o manejo clínico cirúrgico as complicações doença.
منابع مشابه
Porocarcinoma - Relato de caso
Eccrine porocarcinoma is a rare, malignant neoplasm of eccrine sweat glands. It often occurs in elderly people, mean age of 67.5 years. The clinical features are variable and their localization is not related to sweat-gland concentration, occurring mainly on the feet and legs. Disease diagnosis and treatment should be as early as possible in order to avoid tumor aggressiveness that occurs in 20...
متن کاملElaioconiose - Relato de caso
Elaioconiosis is a work-rela ted acnei form der ma to sis which affects the expo sed skin of indi vi duals wor king with oils or grea ses. Its inci den ce has decrea sed with the intro duc tion of per so nal pro tec ti ve equip ment, per so nal hygie ne mea su res and the clea ning of work clo thes. Although not a rare disea se, elaio co nio sis is sel dom repor ted in the lite ra tu re, par ti...
متن کاملMixofibrossarcoma - Relato de caso
Myxofibrosarcoma, previously known as malignant fibrous histiocytoma, myxoid variant, is a rare tumor of mesenchymal origin, composed of spindle cells and myxoid stroma. It mainly affects elderly people, involving the lower extremities and frequently extending to the dermis and subcutaneous tissue. The tumor presents high rates of recurrence, and a deep biopsy is required to obtain the correct ...
متن کاملDeficiência de biotinidase : aspectos clínicos , diagnósticos e triagem neonatal
Biotinidase deficiency is a hereditary metabolic disease with varied phenotypic expression in which there is a defect in the metabolism of biotin. The symptoms of the classic form are often neurological and in the skin, with possible sequelae such as auditory and visual disorders, and motor development and language delay. These manifestations are usually irreversible, even after treatment, whic...
متن کاملDeficiência de alfa1antitripsina: relato de caso
This report draws attention to the alpha 1 antitrypsin deficiency in newborns presented as a cholestatic syndrome. Its sub-diagnosis constitutes a major constraint for recognition and appropriate treatment. Good outcomes occur in approximately 50% of patients. It is associated in most cases, to extra and intra-hepatic involvement and the absence of clinical signs that indicate its diagnosis. Th...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Brazilian Journal of Health Review
سال: 2023
ISSN: ['2595-6825']
DOI: https://doi.org/10.34119/bjhrv6n3-188