Results 151 to 160 of about 87,553 (201)
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Acta Paediatrica, 1973
SummaryTwo siblings, a boy and a girl, with characteristic features of the oculo‐cerebro‐renal syndrome of Lowe are described. In both cases the impaired renal function was a predominant feature of the disease, and both died at the age of 3–4 months.
K B, Cyvin, J, Weidemann, J, Bathen
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SummaryTwo siblings, a boy and a girl, with characteristic features of the oculo‐cerebro‐renal syndrome of Lowe are described. In both cases the impaired renal function was a predominant feature of the disease, and both died at the age of 3–4 months.
K B, Cyvin, J, Weidemann, J, Bathen
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Bulletin des societes d'ophtalmologie de France, 1996
This is a rare syndrome, the exact incidence of which is not known. There are 40 families in the UK recorded as being affected by Lowe’s syndrome. The basic cause of the condition is thought to be some metabolic disorder. The exact nature of this problem is not clear at present, but research into various areas are proceeding in a number of centres. Due
P, FRANCOIS +3 more
+6 more sources
This is a rare syndrome, the exact incidence of which is not known. There are 40 families in the UK recorded as being affected by Lowe’s syndrome. The basic cause of the condition is thought to be some metabolic disorder. The exact nature of this problem is not clear at present, but research into various areas are proceeding in a number of centres. Due
P, FRANCOIS +3 more
+6 more sources
Australian Journal of Mental Retardation, 1970
(1970). Lowe’s Syndrome. Australian Journal of Mental Retardation: Vol. 1, No. 3, pp. 89-93.
Jill Mack, Peter Masters, Athel Hockey
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(1970). Lowe’s Syndrome. Australian Journal of Mental Retardation: Vol. 1, No. 3, pp. 89-93.
Jill Mack, Peter Masters, Athel Hockey
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Other Syndromes: Lowe Syndrome
2016Lowe syndrome (oculocerebrorenal syndrome; OCRL) is a rare (i.e., 1 in 50,0000), X-linked disorder that was first described in 1952. Myriad medical problems arise including complex glaucoma, hypotonia, dental dysfunction, and renal compromise leading to end-stage renal disease in adolescent or adult life.
Donald E. Greydanus +2 more
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2011
Abstract This chapter provides pictures and clinical details of LOWE ...
Roger E. Stevenson +2 more
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Abstract This chapter provides pictures and clinical details of LOWE ...
Roger E. Stevenson +2 more
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Annals of Internal Medicine, 1955
Excerpt Some of the earlier workers noted the presence of low levels of serum sodium or serum total base in pneumonia, diabetes mellitus, eclampsia, uremia, congestive heart failure, cirrhosis and ...
T S, DANOWSKI, E B, GERGUS, F M, MATEER
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Excerpt Some of the earlier workers noted the presence of low levels of serum sodium or serum total base in pneumonia, diabetes mellitus, eclampsia, uremia, congestive heart failure, cirrhosis and ...
T S, DANOWSKI, E B, GERGUS, F M, MATEER
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Transactions of the ophthalmological societies of the United Kingdom, 1981
The histopathological manifestations in four eyes from two male patients with the oculo-cerebro-renal syndrome of Lowe included a small, discoid, cataractous lens, peculiar capsular and epithelial changes with aberrant formation of collagenous fibrous tissue, polar lenticular changes with anterior vitreous condensation, embryonic anterior chamber angle
R C, Tripathi, G W, Cibis, B J, Tripathi
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The histopathological manifestations in four eyes from two male patients with the oculo-cerebro-renal syndrome of Lowe included a small, discoid, cataractous lens, peculiar capsular and epithelial changes with aberrant formation of collagenous fibrous tissue, polar lenticular changes with anterior vitreous condensation, embryonic anterior chamber angle
R C, Tripathi, G W, Cibis, B J, Tripathi
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Wilson’s Syndrome (Low T3 Syndrome)
2019Wilson’s syndrome or “low T3 syndrome” is a pseudo-medical diagnosis that describes a constellation of common and nonspecific symptoms, some of which overlap with that of hypothyroidism. The hallmark of this “disorder” is insufficient T3 that responds to T3 administration.
Catherine J. Tang, Jeffrey R. Garber
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