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PedAM

Pediatric Disease Annotations & Medicines




Disease pulmonary hypertension
Phenotype C0039446|telangiectasia
Sentences 2
PubMedID- 20730251 Following clinical and imagiological evaluation, a diagnosis of pulmonary hypertension (ph) associated with hereditary hemorrhagic telangiectasia (hht) was confirmed.
PubMedID- 23919827 Background: mutations in activin receptor-like kinase-1 (acvrl-1) or endoglin (eng) are mostly identified in patients with hereditary haemorrhagic telangiectasia (hht) associated with pulmonary hypertension (ph), but have not yet been studied in chinese patients.

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