Literature DB >> 1508583

Colour Doppler imaging of intracranial vasculopathy in severe infantile sialidosis.

M Ries1, K H Deeg, D Wölfel, H Ibel, B Maier, G Buheitel.   

Abstract

Neonatal ascites is usually attributed to prenatal infections, lysosomal storage disease and anomalies of the genitourinary tract, gastrointestinal tract or cardiovascular system. We report one case of neonatal ascites associated with infantile sialidosis. Cerebral sonography showed stripe-like intracerebral echogenicities in the region of the basal ganglia. Colour Doppler imaging demonstrated blood flow within the echogenicities confirming the suspected diagnosis of intracranial vasculopathy.

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Year:  1992        PMID： 1508583     DOI： 10.1007/bf02012489

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


  22 in total

Review 1.  Sialidosis: a review of human neuraminidase deficiency.

Authors:  J A Lowden; J S O'Brien
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

2.  Fetal ascites and cytomegalic inclusion disease.

Authors:  D J Frank; W D DeVaux; J R Perkins; E V Perrin
Journal:  Am J Dis Child       Date:  1966-12

Review 3.  Inborn errors of complex carbohydrate metabolism.

Authors:  J Spranger
Journal:  Am J Med Genet       Date:  1987-10

4.  GM1 gangliosidosis presenting as neonatal ascites.

Authors:  K I Abu-Dalu; H Tamary; N Livni; A I Rivkind; S Yatziv
Journal:  J Pediatr       Date:  1982-06       Impact factor: 4.406

5.  Congenital ascites as a presenting sign of lysosomal storage disease.

Authors:  J E Gillan; J A Lowden; K Gaskin; E Cutz
Journal:  J Pediatr       Date:  1984-02       Impact factor: 4.406

6.  Urinary ascites in the newborn.

Authors:  R Kay; R J Brereton; J H Johnson
Journal:  Br J Urol       Date:  1980-12

7.  Neuraminidase deficiency presenting as non-immune hydrops fetalis.

Authors:  M Beck; S W Bender; H L Reiter; W Otto; R Bässler; H Dancygier; J Gehler
Journal:  Eur J Pediatr       Date:  1984-12       Impact factor: 3.183

8.  A severe infantile sialidosis: clinical, biochemical, and microscopic features.

Authors:  A S Aylsworth; G H Thomas; J L Hood; N Malouf; J Libert
Journal:  J Pediatr       Date:  1980-04       Impact factor: 4.406

9.  Neuraminidase deficiency: case report and review of the phenotype.

Authors:  I D Young; E P Young; J Mossman; A R Fielder; J R Moore
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318

10.  Colour flow imaging of the great intracranial arteries in infants.

Authors:  K H Deeg
Journal:  Neuroradiology       Date:  1989       Impact factor: 2.804
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  4 in total

1.  Lenticulostriate echogenic vessels: clinical and sonographic study of 70 neonatal cases.

Authors:  Mayass El Ayoubi; Odile de Bethmann; Michèle Monset-Couchard
Journal:  Pediatr Radiol       Date:  2003-08-01

Review 2.  Type II sialidosis: review of the clinical spectrum and identification of a new splicing defect with chitotriosidase assessment in two patients.

Authors:  A Caciotti; M Di Rocco; M Filocamo; S Grossi; F Traverso; A d'Azzo; C Cavicchi; A Messeri; R Guerrini; E Zammarchi; M A Donati; Amelia Morrone
Journal:  J Neurol       Date:  2009-07-01       Impact factor: 4.849

3.  Neonatal lenticulostriate vasculopathy: further characterisation.

Authors:  I R Makhoul; I Eisenstein; P Sujov; M Soudack; T Smolkin; A Tamir; M Epelman
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2003-09       Impact factor: 5.747

Review 4.  Sialidosis: A Review of Morphology and Molecular Biology of a Rare Pediatric Disorder.

Authors:  Aiza Khan; Consolato Sergi
Journal:  Diagnostics (Basel)       Date:  2018-04-25
  4 in total

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