MALIGNANT HYPERTHERMIA AND NOONAN VERSUS KING SYNDROME

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منابع مشابه

Malignant hyperthermia in a patient with King syndrome.

A case of malignant hyperthermia is reported in a child who subsequently is diagnosed as having King syndrome, a rare genetic disorder first described in 1960. Several unique features associated with this case make it clinically noteworthy. It is important to recognize the patient with King syndrome preoperatively, as King syndrome is a disorder universally linked with the development of malign...

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Malignant Hyperthermia

''Malignant Hypothermia'' syndrome is a rare, but dangerous occurrence, the aetiology of which is not known. Up to this date 180 cases have been reported. This syndrome i's seen generally in :male children over age of two years, and especially in adolescent males. Also those people with muscular abnormalities are more susciptable to this illnes'S. Anaesthetic agent such as halothane or muscular...

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Malignant hyperthermia syndrome in an anxious patient.

A 30-yr-old patient with fulminant ulcerative colitis was anaesthetized on three occasions, for colectomy and rectal stump removal. The first anaesthesia, with droperidol and fentanyl and pancuronium neuromuscular block, was uneventful. Addition of suxamethonium on the second occasion and use of the original drugs plus nitrous oxide for the third anaesthesia produced symptoms of MH, which was c...

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Noonan syndrome.

Noonan syndrome is a common autosomal dominant condition caused by multiple genes in the RasMAPK pathway. The adult phenotype can be extremely subtle, and many adults are diagnosed only after the birth of a more obviously affected child. Whether diagnosis is made in childhood or adulthood, initial and ongoing evaluation of many systems can have considerable health benefits.

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Noonan syndrome

Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital heart defects. The incidence of NS is estimated to be between 1:1000 and 1:2500 live births. The main facial features of NS are hypertelorism with down-slanting palpebral fissures, ptosis and low-set posteriorly rotated ears with a thickened helix. The cardiovascular defects most commonly associa...

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ژورنال

عنوان ژورنال: Pediatric Research

سال: 1984

ISSN: 0031-3998,1530-0447

DOI: 10.1203/00006450-198404001-01279