Abstract
Martsolf's syndrome has been described in Jewish people. We describe a patient of non-Jewish ancestry who has minor differences from other patients. The possible pattern of inheritance is discussed.
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- Lubinsky M. S. Cataracts and testicular failure in three brothers. Am J Med Genet. 1983 Oct;16(2):149–152. doi: 10.1002/ajmg.1320160203. [DOI] [PubMed] [Google Scholar]
- 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]
- Mikati M. A., Najjar S. S., Sahli I. F., Melhem R. E., Mansour S., Der Kaloustian V. M. Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: a new syndrome. Am J Med Genet. 1985 Nov;22(3):599–608. doi: 10.1002/ajmg.1320220319. [DOI] [PubMed] [Google Scholar]
- 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]
- Winter J. S., Taraska S., Faiman C. The hormonal response to HCG stimulation in male children and adolescents. J Clin Endocrinol Metab. 1972 Feb;34(2):348–353. doi: 10.1210/jcem-34-2-348. [DOI] [PubMed] [Google Scholar]