eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | c syndrome |
| Comorbidity | C0025958|microcephaly |
| Sentences | 2 |
| PubMedID- 25606399 | Among the numerous genetic syndromes associated with microcephaly, we specifically aimed at excluding a trisomy of chromosome 21, since this has been linked to both the 47,xyy karyotype (fryns et al., 1995) and microcephaly (korenberg et al., 1994). |
| PubMedID- 22144119 | Infantile nephrotic syndrome with microcephaly and global developmental delay: the galloway mowat syndrome. |
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