| Autor: |
Venkat-Raman, Narayanaswamy, Sebire, Neil J., Murphy, Karl W. |
| Předmět: |
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| Zdroj: |
Fetal Diagnosis & Therapy; 2006, Vol. 21 Issue 3, p250-254, 5p, 2 Charts |
| Abstrakt: |
Hydrops fetalis is associated with a wide range of abnormalities. In about 20% of cases of non-immune fetal hydrops, no cause is found despite investigations including routine post-mortem examination and enzyme studies may be indicated to detect an underlying metabolic storage disease. Fetal hydrops due to mucopolysaccharidosis type VII is very rare and a prenatal diagnosis is not usually made. We report a case of mucopolysaccharidosis type VII presenting as recurrent fetal hydrops and review the clinico-pathological features of this disorder. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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