Literature DB >> 1941968

Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity.

C G Bönnemann1, P Meinecke, H Reich.   

Abstract

Two sibs with an encephalopathy, including intracerebral calcification and white matter lesions, dwarfism owing to growth hormone deficiency, and retinal degeneration are reported. The onset of the disease in both patients occurred with retardation of motor development during the first year of life. Later, dwarfism, mental retardation, spasticity, ataxia, and retinal degeneration became apparent. These cases probably represent some form of connatal leucodystrophy. The differential diagnosis is discussed.

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Year:  1991        PMID: 1941968      PMCID: PMC1017060          DOI: 10.1136/jmg.28.10.708

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  11 in total

1.  Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies.

Authors:  M A Patton; F Giannelli; A J Francis; M Baraitser; B Harding; A J Williams
Journal:  J Med Genet       Date:  1989-03       Impact factor: 6.318

2.  Kearns-Sayre syndrome, hypoparathyroidism, and basal ganglia calcification.

Authors:  A G Dewhurst; D Hall; M S Schwartz; R O McKeran
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-11       Impact factor: 10.154

3.  Two siblings with microcephaly associated with calcification of cerebral white matter.

Authors:  T Ishitsu; S Chikazawa; I Matsuda
Journal:  Jinrui Idengaku Zasshi       Date:  1985-09

4.  Microcephaly and intracranial calcification in two brothers.

Authors:  M Baraitser; E M Brett; A T Piesowicz
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

5.  CAMFAK syndrome: a demyelinating inherited disease similar to Cockayne syndrome.

Authors:  D Talwar; S A Smith
Journal:  Am J Med Genet       Date:  1989-10

6.  A tapetoretinal degeneration with symmetrical calcifications of the basal ganglia. A hereditary disease.

Authors:  W Hammerstein; G Bischof; E Keck
Journal:  Eur Neurol       Date:  1982       Impact factor: 1.710

7.  A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis.

Authors:  J Aicardi; F Goutières
Journal:  Ann Neurol       Date:  1984-01       Impact factor: 10.422

8.  Intracranial calcification in paediatric computed tomography.

Authors:  B Kendall; N Cavanagh
Journal:  Neuroradiology       Date:  1986       Impact factor: 2.804

9.  Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study.

Authors:  A Rodewald; U Froster-Iskenius; E Käb; U Langenbeck; A Schinzel; A Schmidt; E Schwinger; P Steinbach; H Veenema; R D Wegner
Journal:  Clin Genet       Date:  1986-07       Impact factor: 4.438

Review 10.  Encephalopathy with calcifications of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new cases.

Authors:  C Billard; O Dulac; J Bouloche; B Echenne; P Lebon; J Motte; O Robain; J J Santini
Journal:  Neuropediatrics       Date:  1989-02       Impact factor: 1.947

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  1 in total

Review 1.  The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

Authors:  J L Tolmie; P Shillito; R Hughes-Benzie; J B Stephenson
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

  1 in total

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