This paper presents two brothers with incomplete expression of the Smith-Lemli-Opitz syndrome. A definite diagnosis, made after the birth of the second child, could only be reached when the clinical features of both patients were combined.
|Number of pages||8|
|Journal||Acta paediatrica Hungarica|
|Publication status||Published - 1992|
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health