Basal encephalocele and morning glory syndrome.
نویسندگان
چکیده
Basal encephaloceles are often associated with other midline anomalies such as hypertelorism, broad nasal root, cleft lip, and cleft palate. Optic disc anomalies such as pallor, dysplasia, optic pit, coLoboma, and megalopapilla have been reported to occur in patients with basal encephalocele We report a case of a child with a sphenoethmoidal encephalocele and morning glory syndrome of the optic nerve. The presence of such optic nerve anomalies with facial midline anomalies should alert the clinician to the possible presence of a basal encephalocele.
منابع مشابه
Basal encephalocele associated with morning glory syndrome: case report.
The basal encephaloceles refer to rare entities and they correspond to herniation of brain tissue through defects of skull along the cribiform plate or the sphenoid bone. A rare morning glory syndrome, with characteristic retinal defect has been reported in association with basal encephaloceles. Hypophysis hormonal deficiencies may occur. We accounted for a pituitary dwarfism with delayed diagn...
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1. Pierre-Filho Pde T, Limeira-Soares PH, Marcondes AM. Morning glory syndrome associated with posterior pituitary ectopia and hypopituitarism. Acta Ophthalmol Scand. 2004;82:89--92. 2. López-Lizárraga EP, Bolaños-Jiménez R, Treviño-Alanís MG, Rivera-Silva G. Morning glory syndrome. Gac Med Mex. 2011;147:70--1. 3. Tanimoto K, Onda S, Sawaki H, Hiraiwa T, Sano H, Ohnishi M, et al. Hypopituitaris...
متن کاملSpinal epidural abscess in a diabetic patient
1. Pierre-Filho Pde T, Limeira-Soares PH, Marcondes AM. Morning glory syndrome associated with posterior pituitary ectopia and hypopituitarism. Acta Ophthalmol Scand. 2004;82:89--92. 2. López-Lizárraga EP, Bolaños-Jiménez R, Treviño-Alanís MG, Rivera-Silva G. Morning glory syndrome. Gac Med Mex. 2011;147:70--1. 3. Tanimoto K, Onda S, Sawaki H, Hiraiwa T, Sano H, Ohnishi M, et al. Hypopituitaris...
متن کاملAbsence of mutations in Pax6 gene in three cases of morning glory syndrome associated with isolated growth hormone deficiency.
Morning glory syndrome (MGS) is a congenital optic disc dysplasia often associated with craniofacial anomalies, especially basal encephalocele and hypopituitarism. Clinical signs are varied and often occult. The PAX6 gene is involved in ocular morphogenesis and is expressed in numerous ocular tissues during development especially in the developing central nervous system. The aim of the present ...
متن کاملCase Report: Hyperprolactinemia and growth hormone deficiency associated with Morning Glory Syndrome; with a
Morning Glory Syndrome (MGS) is a rare congenital malformation of the optic nerve that is caused by a failure of the closure of the choroidal embryonic fissure . The syndrome is usually seen in association with midline in utero cranial defects, such as transsphenoidal and basal encephaloceles. Although MGS usually presents as an isolated ocular finding, it can be associated with endocrinologic...
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ورودعنوان ژورنال:
- The British journal of ophthalmology
دوره 67 6 شماره
صفحات -
تاریخ انتشار 1983