Disease | marfan syndrome |
Phenotype | C0152021|congenital heart disease |
Sentences | 2 |
PubMedID- 26040324 | Conclusions: taken together, we finalized the diagnosis for this family as x-linked hypophosphatemia (xlh), and diagnosed this girl as marfan syndrome combined with xlh, and congenital heart disease. |
PubMedID- 21776272 | We present a special case of infantile marfan syndrome with a congenital heart disease. |
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