Literature DB >> 2604418

Norrie's disease: a prospective study of development.

H M Goodyear1, P M Sonksen, H McConachie.   

Abstract

Developmental progress, hearing, and dysmorphic features were monitored prospectively in eight babies with Norrie's disease (an X linked form of congenital blindness believed to be associated with mental retardation, regression, sensorineural deafness, and dysmorphic features) and in six congenitally blind peers during their preschool years. No evidence of sensorineural deafness or dysmorphology was found in the group with Norrie's disease. No significant difference in the rate of developmental progress occurred between the two groups. All 14 children showed continuing developmental progress and in 10 this was at a normal or superior rate. Two cases and two controls showed slowing in their rate of progress; in both groups a suboptimal developmental climate had prevailed and may have been contributory. The emphasis on serious and progressive associated disabilities in past reports has led to considerable distress for families of children with this disease. Our study suggests that these anxieties may often be illfounded. Parental depression constrains development, particularly when a baby is blind. More optimistic counselling with developmental guidance is recommended for children who are not overtly retarded in infancy until the long term developmental perspective of this disease is further clarified.

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Year:  1989        PMID: 2604418      PMCID: PMC1792638          DOI: 10.1136/adc.64.11.1587

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  13 in total

1.  Norie's disease (atrofia bulborum hereditaria).

Authors:  M WARBURG
Journal:  Acta Ophthalmol (Copenh)       Date:  1963

2.  Norrie's disease in an Asian family.

Authors:  D G Harendra de Silva; D B de Silva
Journal:  Br J Ophthalmol       Date:  1988-01       Impact factor: 4.638

3.  Norrie's disease in North America.

Authors:  F C Blodi; W S Hunter
Journal:  Doc Ophthalmol       Date:  1969       Impact factor: 2.379

4.  Norrie's disease.

Authors:  M Warburg
Journal:  J Ment Defic Res       Date:  1968-09

5.  A presumptive new variant of Norrie's disease.

Authors:  C A Moreira-Filho; I Neustein
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

6.  Norrie's disease: a study of two families.

Authors:  R M Liberfarb; R D Eavey; G R De Long; D M Albert; J P Dieckert; T Hirose
Journal:  Ophthalmology       Date:  1985-10       Impact factor: 12.079

7.  Norrie's disease: an X-linked syndrome of retinal malformation, mental retardation, and deafness.

Authors:  L B Holmes
Journal:  J Pediatr       Date:  1971-07       Impact factor: 4.406

8.  Norrie's disease--differential diagnosis and treatment.

Authors:  M Warburg
Journal:  Acta Ophthalmol (Copenh)       Date:  1975-03

9.  Norrie disease resulting from a gene deletion: clinical features and DNA studies.

Authors:  D Donnai; R C Mountford; A P Read
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

10.  Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis.

Authors:  A de la Chapelle; E M Sankila; M Lindlöf; P Aula; R Norio
Journal:  Clin Genet       Date:  1985-10       Impact factor: 4.438

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  2 in total

1.  Congenital retinal dystrophies: a study of early cognitive and visual development.

Authors:  M M Black; P M Sonksen
Journal:  Arch Dis Child       Date:  1992-03       Impact factor: 3.791

2.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992
  2 in total

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