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1.
J Pak Med Assoc ; 70(12(B)): 2467-2468, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33475566

ABSTRACT

We report the case of a 12 days old baby boy who presented with swelling and bluish discoloration on his left hip at Pakistan Institute of Medical Sciences in November 2018. Ultrasound (USS) was useful in making the diagnosis of a neonatal psoas abscess. He was treated with extraperitoneal drainage and with systemic antibiotics. The clinical presentation and diagnosis, treatment of this rare condition and brief literature review is given in this case report.


Subject(s)
Psoas Abscess , Staphylococcal Infections , Drainage , Humans , Infant, Newborn , Male , Pakistan , Psoas Abscess/diagnostic imaging , Psoas Abscess/therapy , Staphylococcal Infections/diagnosis , Staphylococcal Infections/drug therapy , Tomography, X-Ray Computed , Ultrasonography
2.
J Pak Med Assoc ; 68(11): 1721-1723, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30410160

ABSTRACT

Bartter syndrome is an autosomal recessive disorder caused by gene mutations that involve hypokalaemia, hypochloraemia and metabolic alkalosis along with raised serum renin, hyperaldosteronism and normal blood pressure. We report two cases of neonatal Bartter syndrome. Case 1 was a product of non-consanguineous marriage and mother had unexplained polyhydramnios in pregnancy while case 2 was a product of consanguineous marriage. Both cases were diagnosed based on hypokalaemia, hypochloraemia and metabolic alkalosis along with elevated serum renin and aldosterone levels. Case 1 positively responded to indomethacin while case 2 had Protein C and S deficiency and sepsis as coexisting diseases and thus could not be given indomethacin and expired. Regular antenatal visits can help in diagnosis of the syndrome particularly if unexplained poly hydramniosis investigated .


Subject(s)
Aldosterone/blood , Bartter Syndrome/diagnosis , Renin/blood , Bartter Syndrome/blood , Biomarkers/blood , Diagnosis, Differential , Humans , Infant, Newborn , Male
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