The anatomical and clinical features of the syndrome are described, and two cases are presented to show that the abnormalities of the different apparatuses, while reflecting a common pathogenetic pattern, may nevertheless vary considerably. Stress is laid on the possibility that the typical facial dysmorphism may be sometimes accompanied by urological alterations that are compatible with life, provided they are recognised and surgically treated in time.
|Translated title of the contribution||Clinical variations in two cases of Potter's syndrome|
|Number of pages||6|
|Publication status||Published - 1980|
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health