dysmorphism

the geneticist documented facial dysmorphism during the initial evaluation.

subtle craniofacial dysmorphism can be missed without a careful physical exam.

the report noted dysmorphism consistent with a known syndrome.

the pediatrician observed dysmorphism and referred the child for genetic testing.

clinical photos were reviewed to assess dysmorphism over time.

mild dysmorphism accompanied developmental delay in several cases.

the team discussed dysmorphism as part of the differential diagnosis.

they described dysmorphism affecting the ears and nasal bridge.

the clinician used standardized terms to describe the dysmorphism.

dysmorphism was not evident, but the family history remained concerning.

further imaging was ordered because skeletal dysmorphism was suspected.

the case series highlighted recurrent patterns of dysmorphism.