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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1992-9-10
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pubmed:abstractText |
Thirty-nine patients (82% under 1 year of age) with Wiedemann-Beckwith syndrome (WBS) were prospectively studied. To evaluate the somatometric data the normal range was set out at mean +/- 2 SD. The relevant physical findings were a characteristic face, non increased mean height and weight, normal head circumference, defective abdominal wall, a predominance of the upper segment, and tibial bowing. Mental retardation was documented in 5 cases but in only 1 it was related to hypoglycemia. The 32 cases karyotyped were normal. Since neonatal hypoglycemia is frequent (34.3% in our series) and potentially deleterious for the CNS we propose to monitor the glycemia every 6 h during the first 3 days in WBS newborns in order to correct glycemia below of 2.6 mmol/l (46.8 mg/dl) according to recent studies. The comparison with previous large series enabled us to precise the frequency, onset and evolution of the main stigmata.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
1015-8146
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
67-76
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pubmed:dateRevised |
2006-7-6
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pubmed:meshHeading |
pubmed-meshheading:1642813-Adolescent,
pubmed-meshheading:1642813-Anthropometry,
pubmed-meshheading:1642813-Beckwith-Wiedemann Syndrome,
pubmed-meshheading:1642813-Bone and Bones,
pubmed-meshheading:1642813-Child,
pubmed-meshheading:1642813-Child, Preschool,
pubmed-meshheading:1642813-Female,
pubmed-meshheading:1642813-Gene Frequency,
pubmed-meshheading:1642813-Humans,
pubmed-meshheading:1642813-Infant,
pubmed-meshheading:1642813-Infant, Newborn,
pubmed-meshheading:1642813-Karyotyping,
pubmed-meshheading:1642813-Male,
pubmed-meshheading:1642813-Mexico,
pubmed-meshheading:1642813-Phenotype,
pubmed-meshheading:1642813-Risk Factors,
pubmed-meshheading:1642813-Tomography, X-Ray Computed
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pubmed:year |
1992
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pubmed:articleTitle |
Wiedemann-Beckwith syndrome: clinical, cytogenetical and radiological observations in 39 new cases.
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pubmed:affiliation |
División de Genética, Instituto Mexicano de Seguro Social, Guadalajara, Jalisco.
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pubmed:publicationType |
Journal Article
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