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Perfil epidemiológico de recém-nascidos com anomalias congênitas no Hospital Universitário Júlio Müller, Mato Grosso, Brasil
(Universidade Federal de Mato GrossoBrasilFaculdade de Medicina (FM)UFMT CUC - CuiabáPrograma de Pós-Graduação em Ciências da Saúde, 2018-05-01)
Congenital anomaly (CA) is a functional or structural anomaly of fetal
development due to a factor that originates before birth, whether genetic,
environmental or unknown, even when the defect is not apparent in the ...
Anomalia gravimétrica do flanco sul do alto estrutural de Pau D'Alho
(Universidade Estadual Paulista (Unesp), 2014)
This work present the results from a geophysical survey (gravimetric method) of the accentuated gravimetric anomaly between Pau d'Alho and Anhembi structural highs, in the geological context of the Northeast Limb of the ...
Pectus carinatum in a Cat
(Universidade Federal do Rio Grande do Sul, 2019)
Possible New Syndrome: Left Ventricular Noncompaction, Partial Agenesis of the Corpus Callosum, and Developmental Delay in a Brazilian Child
(Wiley-liss, 2009-05-01)
We report oil the clinical, neuropsychological and language characteristics of it boy with left ventricular noncompaction cardiomyopathy (LVNC), agenesis of the splenium of the corpus callosum, minor anomalies of face and ...
Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families.
(1986-12-01)
We report on five Brazilian patients from three unrelated families with congenital anomalies of the upper limbs. Ulnar aplasia/hypoplasia was the main reason for examining these patients. Evidence for existence of an ulnar ...
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly
(Elsevier B.V., 2010-03-01)
Holoprosencephaly (HPE) is a malformation sequence where the cerebral hemispheres fail to separate into distinct left and right halves. It can be associated with midline structural anomalies of the central nervous system ...
Possible New Syndrome: Left Ventricular Noncompaction, Partial Agenesis of the Corpus Callosum, and Developmental Delay in a Brazilian Child
(Wiley-liss, 2009-05-01)
We report oil the clinical, neuropsychological and language characteristics of it boy with left ventricular noncompaction cardiomyopathy (LVNC), agenesis of the splenium of the corpus callosum, minor anomalies of face and ...
Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
(Wiley-Blackwell, 2003-09-15)
The Richieri-Costa-Pereira syndrome is a rare autosomal recessive disorder characterized by short stature, Robin sequence, cleft mandible, pre/postaxial anomalies and clubfoot. of 15 families reported with this disorder ...
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly
(Elsevier B.V., 2010-03-01)
Holoprosencephaly (HPE) is a malformation sequence where the cerebral hemispheres fail to separate into distinct left and right halves. It can be associated with midline structural anomalies of the central nervous system ...