INTRODUCTION Lowe oculocerebrorenal syndrome is a rare X-linked disorder characterized by  study abnormalities of the lens,   channeliseland and kidneys. It leads to the clinical triad of cataract formation during early infancy, mental   slowdown and a broad range of renal abnormalities, including incomplete  total heat carbonate resumption, renal tubular acidosis and end-st time kidney disease (Lowe, Terrey, MacLachan, 1952, 83:164-84.)[1, 2]. The OCRL1  factor is  find on chromosome Xq25-26(Lowe, Terrey, MacLachan, 1952, 83:164-84.)1 .Over 70 mutations have been identified. ( Charnas & deoxyadenosine monophosphate; Gahl, 1990; 38:75-107.)2 The OCRL gene encodes phosphatidylinositol 4, 5-biphospsphate 5-phosphatase (ocrl1p) is present in the Golgi complex, and reduced enzyme  natural action results in increased enzyme substrate and abnormal distribution of acting-binding proteins that  may  stool abnormal cell migration and differentiation.( Suchy & Nussbaum, 2002;71:1420-1427)4    clinical REPORT This boy was the  fleck child of non-consanguineous healthy parents and had a birth weight of 2.9 kg at 40 weeks of gestation. He had generalized hypotonia and  inseparable cataracts after birth. Cranial  sonography showed features of generalized brain atrophy. Chromosome  analysis showed a normal 46,XY  manlike karyotype and the TORCH screen was negative.  nephritic and abdominal ultrasound findings were unremarkable. His psychomotor development was severe delay, with  sitting unsupported at 14 months, independent ambulation at 2 years and speaking his  starting time words at 2 years. He was diagnosed as Lowe syndrome until age 4 years 10 months when he developed  metabolic acidosis after lower airway infection. On examination, his height, weight and occipital  facade circumference below the fifth percentile for age. The  nerve was triangular in appearance; the head was dolichocephalic with frontal bossing; hairline was receded anteriorly. The eyes were deeply set.    The ears were large, protruding, but  unrem!   arkably placed. The palate was  super arched. The philtrum was prominent and elongated; the upper  oral fissure was thin. He had numerous dental carries, some of...                                        If you want to  fill a full essay, order it on our website: BestEssayCheap.com
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