Sentence examples for more clinical features from inspiring English sources

More clinical features differ between UC and CD.

Only 5/174 (2.9%) infants had two or more clinical features of EONS and one of these infants also had a temperature >38°C.

In this case, the differential diagnosis had 1,136 rows, representing 597 genes, of which 222 matched two or more clinical features.

On presentation, 12 had cerebral malaria (35%), 10 had respiratory distress (29%), 6 had acute renal impairment (18%) and 12 (35%) had 2 or more clinical features of severe malaria (table 3).

PHR features can range from administrative (e.g. booking appointments and paying bills) to more clinical features (e.g. reviewing information, communicating with the care team, documenting care activities/results/outcomes).

For inclusion, patients had to have one or more clinical features consistent with the CF phenotype [ 12] as well as a genotype with two identifiable disease-causing CF transmembrane conductance regulator (CFTR) mutations and sweat chloride measurements greater than 60 mmol/L on two occasions.

Compared with patients with deletional Hb H disease, patients with nondeletional Hb H disease had more severe clinical features, including a younger age at diagnosis, more requirement of blood transfusions, and a larger proportion of patients with splenomegaly, hepatomegaly, or jaundice.

Men with CD are more likely to present at a younger age with more florid clinical features.

After further investigation of the genotype-phenotype correlation in 68 patients, we found that patients with nondeletional Hb H disease had more severe clinical features than those with deletional Hb H disease, including younger age at diagnosis, more requirement of blood transfusions, and larger proportion of patients with splenomegaly, hepatomegaly or jaundice.

Changes of neurosteroids concentrations in CH patients were significant only for AP, which may contribute to the more severe clinical features of CH vs CM and EM.

The 17p13.1 microdeletion syndrome is a recently described genomic disorder with a core clinical phenotype of intellectual disability, poor to absent speech, dysmorphic features, and a constellation of more variable clinical features, most prominently microcephaly.