Buscar
Mostrando ítems 1-10 de 1123
Hearing disorders in congenital toxoplasmosis: A literature review
(2018-07-01)
Introduction Several studies show correlations between congenital toxoplasmosis and hearing loss, with a broad diversity of levels of hearing loss and specifications of hearing disorders. Objective To describe the studies ...
Spatial Distribution of Congenital Disorders Diagnosed by the Newborn Screening Program in Ecuador
(2021)
The newborn screening program in Ecuador has been operating since 2011 under the responsibility of the Ministry of Health. This program is centralized and diagnoses four diseases: congenital hypothyroidism, phenylketonuria, ...
Bilateral clinical anophthalmia associated with congenital hydrocephalus in the dog
(Univ Federal Santa Maria, 2011-07-01)
The complete absence of the eyeball is rare in dogs and cats, and hydrocephalus is commonly seen as a congenital disorder in toy or brachycephalic dogs before one year old. This paper describes for the first time in Brazil ...
Sleep in infants with congenital heart disease
(Faculdade de Medicina / USP, 2009)
OBJECTIVES: To investigate hypoxia and sleep disordered breathing in infants with congenital heart disease. METHODS: Prospective study. In-hospital full polysomnography was performed on 14 infants with congenital heart ...
Anoftalmia clínica bilateral associada à hidrocefalia congênita em cão
(2011-07-01)
The complete absence of the eyeball is rare in dogs and cats, and hydrocephalus is commonly seen as a congenital disorder in toy or brachycephalic dogs before one year old. This paper describes for the first time in Brazil ...
Atrichia, abnormal EEG, epilepsy and mental retardation in two sisters
(Karger, 1979-01-01)
Two daughters of a nonconsanguineous couple are described. Both present mental retardation, epileptic seizures, congenital atrichia, histologically anomalous skin and abnormal EEG pattern. From a discussion of the literature ...
Dry eye in childhood: Epidemiological and clinical aspects
(ETHIS COMMUNICATINS, INCEstados Unidos, 2008)
Hypomyelination and Congenital Cataract: Identification of a Novel likely pathogenic c.414+1G>A in FAM126A gene Variant
(Wiley, 2021)
It is key to expand the differential diagnosis and consider possible genetic etiologies on a patient with congenital cataracts associated with clinical features, such as leukodystrophy or polyneuropathy.