Literature DB >> 6303272

[Ultrastructural findings in 9 fetuses following prenatal diagnosis of neurolipidoses].

G Suchlandt, W Schlote, K Harzer.   

Abstract

After positive prenatal enzymic diagnosis of different neurolipidoses therapeutic abortion was carried out in the 19th to 25th week of pregnancy. Ten delivered fetuses were studied ultrastructurally and in nine of them positive results were obtained, although in some cases one had to accept relatively poor structural conservation of fetal tissues. The ultrastructure of the quantitatively small lipid storage effects qualitatively resembled that of the postnatal stages with some exceptions of localization. In fetal GM2-gangliosidosis type 2 (variant 0) concentric membranous cytoplasmic bodies were detected in the brain cortex. In Krabbe's disease the myelinated regions of the spinal cord showed scattered storage (globoid) cells, sometimes closely related to blood vessels, which contained isolated or stranded tubular or spicular inclusions. In GM1-gangliosidosis type 1 neurons of the brain stem showed lamellar inclusions structured as zebra bodies, and splenic histiocytes exhibited numerous almost clear cytoplasmic vacuoles. In fetal metachromatic leukodystrophy the CNS including myelinated regions was essentially free of morphologic lipid storage effects. However, many kidney tubules cells contained great numbers of irregular or roughly parallel stacks of membranes. These inclusions may be equivalent to "tuffstone" bodies. In one fetus the bodies were restricted to tubular cells bearing microvilli. Fluorescent microscopy of arcus of the kidney tubule showed excess amounts of metachromatic material. Less of this material was demonstrable in the envelope layer of hepatic Glisson triangles. In the fetus with Niemann-Pick disease type C large neurons of the basal ganglia and the spinal cord were filled with membranous inclusions that were similar to myelin-shaped bodies rather than to solid membraneous bodies. The 19-weeks-old fetus with enzymically proven Gaucher disease was free of ultrastructural lipid storage effects. Most but not all of the morphological findings in the fetuses with neurolipidoses were in accordance with published results.

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Mesh:

Year:  1982        PMID: 6303272     DOI: 10.1007/bf00345597

Source DB:  PubMed          Journal:  Arch Psychiatr Nervenkr (1970)


  23 in total

1.  Studies in Tay-Sachs disease. IV. Membranous cytoplasmic bodies.

Authors:  S SAMUELS; S R KOREY; J GONATAS; R D TERRY; M WEISS
Journal:  J Neuropathol Exp Neurol       Date:  1963-01       Impact factor: 3.685

2.  [Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)].

Authors:  K Harzer; S Stengel-Rutkowski; E O Gley; A Albert; J D Murken; V Zahn; K P Henkel
Journal:  Dtsch Med Wochenschr       Date:  1975-01-17       Impact factor: 0.628

3.  Neurovisceral lipidosis compatible with Niemann-Pick disease type C: morphological and biochemical studies of a late infantile case and enzyme and lipid assays in a prenatal case of the same family.

Authors:  K Harzer; W Schlote; J Peiffer; H U Benz; A P Anzil
Journal:  Acta Neuropathol       Date:  1978-08-07       Impact factor: 17.088

4.  Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction-dependent: evidence for a component defect in Niemann-Pick disease type C is spurious.

Authors:  K Harzer; A P Anzil; I Schuster
Journal:  J Neurochem       Date:  1977-12       Impact factor: 5.372

Review 5.  [Prenatal diagnosis of incurable familial metabolic diseases. Prenatal diagnosis of disorders of lipid metabolism].

Authors:  K Harzer
Journal:  Med Welt       Date:  1979

6.  Sequence of morphological alterations in the nervous system of metachromatic leucodystrophy. Light- and electronmicroscopic observations in the central and peripheral nervous system in a prenatally diagnosed foetus of 22 weeks.

Authors:  C Meier; A Bischoff
Journal:  Acta Neuropathol       Date:  1976-12-21       Impact factor: 17.088

7.  Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy family.

Authors:  G Dubois; K Harzer; N Baumann
Journal:  Am J Hum Genet       Date:  1977-03       Impact factor: 11.025

8.  Enzymic diagnosis in 27 cases with Gaucher's disease.

Authors:  K Harzer
Journal:  Clin Chim Acta       Date:  1980-09-08       Impact factor: 3.786

9.  Metachromatic reaction of pseudoisocyanine with sulfatides in metachromatic leukodystrophy (MLD). I. Technique of histochemical staining.

Authors:  H U Benz; K Harzer
Journal:  Acta Neuropathol       Date:  1974-02-28       Impact factor: 17.088

10.  Fetal Krabbe leukodystrophy. A morphologic study of two cases.

Authors:  J J Martin; J G Leroy; C Ceuterick; J Libert; P Dodinval; L Martin
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

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