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. 1979 Aug;16(4):309–313. doi: 10.1136/jmg.16.4.309

Night blindness, characteristic facies, and skeletal abnormalities in two brothers.

A G Hunter, D R Thompson, M H Reed, A G Macrodimitris
PMCID: PMC1012676  PMID: 314984

Abstract

Two brothers are described with a similar physical appearance characterised by minor periorbital anomalies, malar flatness, a maxillary overbite, retrognathia, sloping shoulders, joint hyperextensibility, and minor radiological anomalies. In addition, they had a slowly progressing night blindness, myopia, and extinguished electroretinograms. The mother had mild expression of some of the physical anomalies and a decreased electroretinogram response to red light. We have been unable to find any report of similarly affected children. The possible modes of inheritance are discussed.

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Selected References

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  1. ANTOINE B., BRAUN-VALLON S., d' ANGLEJEAU, PERRIN D., DUNOD J. P., RYCKEWAERT A. [Familial nephropathy with bone and chorioretinal involvement]. J Urol Nephrol (Paris) 1963 Jan-Feb;69:81–89. [PubMed] [Google Scholar]
  2. François J., De Rouck A. Sex-linked myopic chorioretinal heredodegeneration. Am J Ophthalmol. 1965 Oct;60(4):670–678. doi: 10.1016/0002-9394(65)92258-0. [DOI] [PubMed] [Google Scholar]
  3. Herrmann J., France T. D., Spranger J. W., Opitz J. M., Wiffler C. The Stickler syndrome (hereditary arthroophthalmopathy). Birth Defects Orig Artic Ser. 1975;11(2):76–103. [PubMed] [Google Scholar]
  4. Mainzer F., Saldino R. M., Ozonoff M. B., Minagi H. Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities. Am J Med. 1970 Oct;49(4):556–562. doi: 10.1016/s0002-9343(70)80051-1. [DOI] [PubMed] [Google Scholar]
  5. Pearlman J. T., Flood T. P., Seiff S. R. Retinitis pigmentosa without pigment. Am J Ophthalmol. 1976 Apr;81(4):417–419. doi: 10.1016/0002-9394(76)90296-8. [DOI] [PubMed] [Google Scholar]
  6. Popović-Rolović M., Calić-Perisíc N., Bunjevacki G., Negovanović D. Juvenile nephronophthisis associated with retinal pigmentary dystrophy, cerebellar ataxia, and skeletal abnormalities. Arch Dis Child. 1976 Oct;51(10):801–803. doi: 10.1136/adc.51.10.801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Villaverde M. M., da Silva J. A. Distal brachyphalangy of the thumb in mental retardation. J Med Genet. 1975 Dec;12(4):401–404. doi: 10.1136/jmg.12.4.401. [DOI] [PMC free article] [PubMed] [Google Scholar]

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