Alagille syndrome

A rare syndrome variably characterized by chronic cholestasis due to paucity of intrahepatic bile ducts, peripheral pulmonary artery stenosis, vertebrae segmentation anomalies, characteristic facies, posterior embryotoxon/anterior segment abnormalities, pigmentary retinopathy, and dysplastic kidneys.

Hemiparesis

Loss of strength in the arm, leg, and sometimes face on one side of the body. Hemiplegia refers to a complete loss of strength, whereas hemiparesis refers to an incomplete loss of strength.


合計: 1

                      


(表示件数)
PMID (PMCID)
2750789
FEMALE Infant
Alagille syndrome associated with moyamoya disease.
Rachmel A, Zeharia A, Neuman-Levin M, Weitz R, Shamir R, Dinari G.
Am J Med Genet. 1989;33(1):89-91.
A 22-month-old girl with the typical manifestations of Alagille syndrome presented with acute right hemiparesis.