Document Detail


Stickler syndrome in Pierre-Robin sequence prenatal ultrasonographic diagnosis and postnatal therapy: two cases report.
MedLine Citation:
PMID:  21375138     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Pierre-Robin Syndrome (PRS) is a rare congenital abnormality, with an approximately 1/30,000 estimated rate, characterized by the presence of the combination of mandibular hypoplasia (micrognathia or small jaw), glossoptosis (retrusion of the tongue into the pharyngeal airway) and, often, a posterior cleft of the secondary palate. It may be an isolated occurrence or part of a more complex syndrome and it is associated with long-term respiratory, nutritional, and developmental difficulties. Stickler syndrome (SS) is a rare autosomal dominant connective tissue disorder estimated to affect approximately 1/7500 newborns. It is diagnosed clinically and, at present, there is no consensus on a minimal clinical diagnostic criterion. The most frequent diagnosis in patients with syndromic Pierre Robin sequence is Stickler syndrome, which may be complicated by congenital high myopia and substantial risk of retinal detachment. However, cases of Stickler syndrome with probable visual complications are rarely identified among this group of patients by members of the cleft team. The patient had an acute unilateral hydrops, with a monolateral keratoconus. The ocular abnormalities included: severe myopia, abnormalities of the vitreous, and high risk of retinal detachment (with subsequent blindness). We report two extremely rare cases of prenatal diagnosis of PRS and SS, prematurely identified by prenatal ultrasonography and successively managed by oculists ophthalmogists.
Authors:
E Pacella; A Malvasi; A Tinelli; F Laterza; D Dell'Edera; F Pacella; F Mazzeo; A Ferraresi; K G Malarska; C Cavallotti
Related Documents :
2821448 - Cushing's syndrome caused by an ectopic pituitary adenoma.
8191648 - Cushing's syndrome secondary to olfactory neuroblastoma.
18379368 - Difficulties in diagnosis and management of ectopic cushing syndrome.
8323178 - An overview of the diagnostic considerations in polycystic ovarian syndrome.
8775418 - Fg syndrome: the trias mental retardation, hypotonia and constipation reviewed.
8275278 - Involvement of opioid mechanisms in the dorsal periaqueductal gray in drug abuse.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  European review for medical and pharmacological sciences     Volume:  14     ISSN:  1128-3602     ISO Abbreviation:  Eur Rev Med Pharmacol Sci     Publication Date:  2010 Dec 
Date Detail:
Created Date:  2011-03-07     Completed Date:  2011-03-23     Revised Date:  2012-01-20    
Medline Journal Info:
Nlm Unique ID:  9717360     Medline TA:  Eur Rev Med Pharmacol Sci     Country:  Italy    
Other Details:
Languages:  eng     Pagination:  1051-4     Citation Subset:  IM    
Affiliation:
Department of Ophtalmology, Sapienza University, Rome, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / therapy,  ultrasonography*
Adult
Connective Tissue Diseases / congenital,  therapy,  ultrasonography*
Female
Humans
Infant, Newborn
Male
Myopia / congenital,  therapy,  ultrasonography*
Pierre Robin Syndrome / therapy,  ultrasonography
Predictive Value of Tests
Retinal Detachment / congenital,  therapy,  ultrasonography*
Treatment Outcome
Ultrasonography, Prenatal*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Opioid-related bowel dysfunction: prevalence and identification of predictive factors in a large sam...
Next Document:  Effects of Azadirachta indica on certain hematological parameters during benzo(a)pyrene induced muri...