COMPLICATED PRESENTATION OF PIERRE ROBIN SYNDROME- A CASE REPORT

سندرم پیرروبین ( THE PIERRE ROBIN SYNDROME )

Role of SOX9 in the Etiology of Pierre-Robin Syndrome

Objective(s:Cleft lip/palate are common congenital anomalies, affecting approximately 2/1000 live births. Pierre Robin Sequence is a subgroup of the cleft palate population. Chromosomal abnormalities near the SOX9 gene disrupt the regulation of this gene and prevent the SOX9 protein from properly controlling the development of facial structures, which leads to isolated PRS. The present study wa...

Unusual presentation of the Conn\'s syndrome: a case report

 Abstract A 26 -year- old woman presented with rhabdomyolysis secondary to severe hypokalemia. Hypertension and metabolic alkalosis could lead to the suspicion of primary aldosteronism, which was confirmed by a decreased plasma rennin, elevated plasma aldosterone levels and high aldosterone/rennin ratio additionally. Additionally adrenal computed tomography showed an adrenal tumour. Blood press...

The Robin anomalad (Pierre Robin syndrome)--a follow up study.

During a 10-year period 55 patients with the Robin anomalad were admitted to the Liverpool Regional Cleft Palate Units. Fourteen (25%) children died. All deaths were within 3 months of birth. Congenital abnormalities other than mandibular retrognathia and cleft palate were present in 14 (26%) children. Peripheral limb defects were particularly common. Thirty children were recalled and reviewed ...

Case Report Pierre Robin Syndrome: A Rare Genetic Disorder and its Dental Management

Relatively very few number of Pierre Robin syndrome patients are affected by genetic syndromes that involve oral structures or the structures associated with first brachial arch. This case report markedly emphasizes the dental management of children with Pierre Robin syndrome. A 7 years old boy had been referred to the outpatient department with complaint of pain and decayed teeth, description ...