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1.
East Mediterr Health J ; 16(2): 214-7, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20799577

RESUMO

This study aimed to determine the possible etiology ot ambiguous genitalia in 41 newborn intants at a referral hospital in Hofuf city, Saudi Arabia. In 46,XX karyotype patients (n 14), congenital adrenal hyperplasia and general malformation disorder were the most common causes of genital ambiguity, while in 46,XY karyotype patients (n=18), testosterone pathway biosynthetic defect was the most common cause even in conjunction with a generalized malformation disorder. In patients with abnormal karyotype (n=3), 1 had trisomy 18 (47,XX) and died after 3 months and 2 had different types of mosaic Turner syndrome. The karyotype was undetermined in 6 natients. Positive family history of ambiguous genitalia was noted in 4 patients.


Assuntos
Transtornos do Desenvolvimento Sexual/epidemiologia , Genitália/anormalidades , Anormalidades Múltiplas/epidemiologia , Anormalidades Múltiplas/genética , Hiperplasia Suprarrenal Congênita/complicações , Hiperplasia Suprarrenal Congênita/epidemiologia , Hiperplasia Suprarrenal Congênita/genética , Causalidade , Transtornos do Desenvolvimento Sexual/diagnóstico , Transtornos do Desenvolvimento Sexual/genética , Síndrome de Frasier/complicações , Síndrome de Frasier/epidemiologia , Síndrome de Frasier/genética , Síndrome de Goldenhar/complicações , Síndrome de Goldenhar/epidemiologia , Síndrome de Goldenhar/genética , Hospitais Urbanos , Humanos , Recém-Nascido , Cariotipagem , Linhagem , Estudos Prospectivos , Encaminhamento e Consulta , Arábia Saudita/epidemiologia , Trissomia/patologia , Síndrome de Turner/complicações , Síndrome de Turner/epidemiologia , Síndrome de Turner/genética , População Urbana/estatística & dados numéricos
2.
(East. Mediterr. health j).
em Inglês | WHO IRIS | ID: who-117845

RESUMO

This study aimed to determine the possible etiology of ambiguous genitalia in 41 newborn infants at a referral hospital in Hofuf city, Saudi Arabia. In 46,XX karyotype patients [n = 14], congenital adrenal hyperplasia and general malformation disorder were the most common causes of genital ambiguity, while in 46,XY karyotype patients [n = 18], testosterone pathway biosynthetic defect was the most common cause even in conjunction with a generalized malformation disorder. In patients with abnormal karyotype [n = 3], 1 had trisomy 18 [47,XX] and died after 3 months and 2 had different types of mosaic Turner syndrome. The karyotype was undetermined in 6 patients. Positive family history of ambiguous genitalia was noted in 4 patients


Assuntos
Estudos Prospectivos , Hiperplasia Suprarrenal Congênita , Diferenciação Sexual , Testosterona , Cariotipagem , Genitália
3.
Libyan Journal of Medicine ; 3(1): 1-4, 2008.
Artigo em Inglês | AIM (África) | ID: biblio-1265030

RESUMO

Objective: To determine the rate and the type of ventriculoperitoneal (VP) shunt infections in infants and children admitted to King Fahad Hofuf hospital of Al-Ahsaa area at the Eastern Province of Saudi Arabia. Methods: From mid 2003 to end of 2006; VP shunt infection episodes were reviewed. Once infection was suspected; a cerebro- spinal fluid (CSF) sample was taken and empirical antibiotics were recommended. Once infection was confirmed; VP shunt was removed and external ventricular drainage (EVD) was inserted until CSF became sterile after which a new shunt was inserted. Results : 25.9 of patients with VP shunts had infections which represents 29.3of the procedures. 40 of infected patients had recurrent episodes. 59.1 of infections occurred throughout the first two months following insertion. Single pathogen was isolated in each episode. Pseudomonas auerginosa represented 50 of isolated pathogens compared with 18.2 with Staphylococcus epidermidis. Conclusions There is a high incidence of VP shunt infections in King Fahad Hofuf hospital when compared with other international centres. Gram negative organisms are the most common cause of the infection


Assuntos
Infecções Bacterianas , Criança , Lactente , Derivação Ventriculoperitoneal
5.
Libyan j. med ; 2(2)2007.
Artigo em Inglês | AIM (África) | ID: biblio-1265054

RESUMO

Objective: To determine predictors for outcomes of traumatic brain injury (TBI) in infants and children younger than twelve years admitted to our pediatric intensive care units (PICU).Methods: This is a retrospective cohort study from 2004-5; done at the PICU of King Fahad Hofuf Hospital; Eastern Province; Saudi Arabia. One hundred and six patients with TBI; 65 boys and 41 girls ages 12 or under; with a mean age of 5.7 years; were included. Of them; 11.3died (Deaths group); 11survived with neurological deficits (ND-group); and 77survived with no neurological deficits (NND-group). The potential predictors for death or neurological deficits were examined.Results: 83of deaths had initial Glascow coma scale (GCS) of = 4/15; 50of ND had initial GCS = 8 and 27of NND had GCS 12. The initial brain CT was abnormal in 92of deaths and ND groups; but in only 37of NND. Combined brain pathologies were found in 92of deaths; 63of ND and only in 5of NND. Hypotension was seen in 67of deaths; 17ND and only in 1of NND. Mechanical ventilation was required in all deaths and more than half of ND. Liver enzymes were high in 50of deaths and 66of ND but in only 20of NND. Serum albumin was low in 33of deaths; 42of ND and only 1NND.Conclusion: Glasgow coma score; brain CT findings; combined brain pathologies; hypotension; high liver enzymes and low serum albumin predict outcome after TBI in pediatric age group


Assuntos
Lesões Encefálicas , Criança , Coma , Traumatismos Craniocerebrais
6.
(East. Mediterr. health j).
em Inglês | WHO IRIS | ID: who-117290

RESUMO

We determined the incidence, etiology and outcome of paediatric coma patients in King Fahad Hospital, which is the only referral centre for Al-Hasa region, Saudi Arabia. From April 1999 to March 2002, 91 children with coma [age range 28 days to 12 years] were admitted. The Glasgow Coma Scale for children was used for assessment. Neurological outcomes were categorized as intact, impairment or death. Incidence of coma was 4.77 per 100 000 population per year. Trauma [head trauma or polytrauma] was the commonest cause of coma [52.8%], followed by infection [25.3%]. Mortality was 47.2% [35.4% among traumatic cases and 60.5% among non-traumatic cases]. There was impaired outcome in 19.8% of patients [22.9% with traumatic coma and 16.3% with non-traumatic coma]


Assuntos
Coma , Tomografia Computadorizada por Raios X , Prognóstico , Escala de Coma de Glasgow , Estudos Retrospectivos
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