Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1989 Jun;26(6):397–400. doi: 10.1136/jmg.26.6.397

Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndrome.

M G Harbord 1, M Baraitser 1, J Wilson 1
PMCID: PMC1015627  PMID: 2738902

Abstract

The association of microcephaly, mental retardation, cataracts, and hypogonadism is described in sibs (brother and sister) of consanguineous parents. These features are consistent with a diagnosis of Martsolf's syndrome. In addition, one sib had a cardiomyopathy while the other had cardiac failure.

Full text

PDF
397

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Donaldson M. D., Warner A. A., Trompeter R. S., Haycock G. B., Chantler C. Familial juvenile nephronophthisis, Jeune's syndrome, and associated disorders. Arch Dis Child. 1985 May;60(5):426–434. doi: 10.1136/adc.60.5.426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Frydman M., Kauschansky A., Leshem I., Savir H. Oculo-palato-cerebral dwarfism: a new syndrome. Clin Genet. 1985 Apr;27(4):414–419. doi: 10.1111/j.1399-0004.1985.tb02286.x. [DOI] [PubMed] [Google Scholar]
  3. Hennekam R. C., van de Meeberg A. G., van Doorne J. M., Dijkstra P. F., Bijlsma J. B. Martsolf syndrome in a brother and sister: clinical features and pattern of inheritance. Eur J Pediatr. 1988 Jun;147(5):539–543. doi: 10.1007/BF00441986. [DOI] [PubMed] [Google Scholar]
  4. Lowry R. B. Editorial comment: variability in the Smith-Lemli-Opitz syndrome: overlap with the Meckel syndrome. Am J Med Genet. 1983 Mar;14(3):429–433. doi: 10.1002/ajmg.1320140305. [DOI] [PubMed] [Google Scholar]
  5. Martsolf J. T., Hunter A. G., Haworth J. C. Severe mental retardation, cataracts, short stature, and primary hypogonadism in two brothers. Am J Med Genet. 1978;1(3):291–299. doi: 10.1002/ajmg.1320010305. [DOI] [PubMed] [Google Scholar]
  6. Strisciuglio P., Costabile M., Esposito M., Di Maio S. Martsolf's syndrome in a non-Jewish boy. J Med Genet. 1988 Apr;25(4):267–269. doi: 10.1136/jmg.25.4.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Sánchez J. M., Barreiro C., Freilij H. Two brothers with Martsolf's syndrome. J Med Genet. 1985 Aug;22(4):308–310. doi: 10.1136/jmg.22.4.308. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES