Deafness and the Laurence-Moon-Biedl Syndrome
Open Access
- 1 February 1950
- journal article
- research article
- Published by BMJ in British Journal of Ophthalmology
- Vol. 34 (2), 65-88
- https://doi.org/10.1136/bjo.34.2.65
Abstract
2 families of this syndrome are reported. In the first family the parents were first cousins. There were 9 children[long dash]2 females showing the complete syndrome, 1 female who died young but is alleged to have had polydactyly, 2 male deaf mutes with no signs of the syndrome, 2 normal females and 2 normal males. A survey of the literature shows that deaf mutism in Laurence-Moon-Biedl cases and their sibs is 30 times as high as in the general population. In the second family the parents were unrelated. There were 2 children- -1 female showing the complete syndrome, and 1 male showing the syndrome except for polydactyly.Keywords
This publication has 20 references indexed in Scilit:
- Zur Kenntnis des Laurence-Moon-Biedl'schen SyndromsEuropean Neurology, 1946
- LAURENCE-MOON-BIEDL SYNDROMEAmerican Journal of Diseases of Children, 1942
- HEREDOFAMILIAL DEVIATIONSAmerican Journal of Diseases of Children, 1940
- On Laurence‐Moon‐Biedl's SyndromeActa Medica Scandinavica, 1940
- Über Störungen des Wasserhaushalts bei zwei Kranken mit dem Lawrence-Moon-Biedlschen SyndromZeitschrift für Neurologie, 1938
- A MELANOSOME-DISPERSING SUBSTANCE IN THE BLOOD AND URINE OF PATIENTS WITH RETINITIS PIGMENTOSA (Preliminary Communication)British Journal of Ophthalmology, 1938
- THE LAURENCE-BIEDL SYNDROME OCCURRING IN A BROTHER AND SISTERArchives of Neurology & Psychiatry, 1938
- LAURENCE-MOON-BIEDL SYNDROMEArchives of Internal Medicine, 1938
- CEREBRAL ADIPOSITY WITH NERVE DEAFNESS, MENTAL DEFICIENCY AND GENITAL DYSTROPHYThe American Journal of the Medical Sciences, 1932
- SOME NEW PEDIGREES OF HEREDITARY DISEASEAnnals of Eugenics, 1930