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Case Report
A Case of Arthrogryposis Multiplex Congenita with Congenital Hypertropic Pyloric Stenosis
Seung Chul Yang, So Young Kim, Hyun Hi Kim, Seung Hoon Han, Jong In Byun, Won Bae Lee
Clin Exp Pediatr. 1995;38(11):1577-1582.   Published online November 15, 1995
Arthrogryposis multiplex congenita is a congenital syndrome characterized by extreme stiffness and contracture of multiple joints and associated hypoplasia or absence of development of muscle, bone, and soft tissues; and refers to a heterogeneous group of congenital disorders of unknown but probably multiple etiologies. We present a 50 days old male baby who has had mmultiple fixed contractures of joints...
A Case of Rhizomelic Chondrodysplasia Punctata
Yeon Dong Lee, Moon Young Song, Hyun Hi Kim, Seunghoon Han, Wonbae Lee
Clin Exp Pediatr. 1994;37(9):1312-1316.   Published online September 15, 1994
Chondrodysplasia punctata is a rare congenital disorder of bone, occuring in infants, which is characterized by raiographic manifestation of premature deposition of punctate calcific densitiy in epiphyseal areas, preformed in carilage. We experienced a case of rhizomelic type-chondrodysplsia punctata in a two day old female who showed short stature, symmetric shortening of proximal limbs, cataract, icthyositic skin lesion and characteristic coronal...
A Case of Broad QRS Paroxysmal Supraventricular Tachycardia That is Difficult to Differentiate from Ventricular Tachycardia
Hung Ki Min, Hyun Hi Kim, Jong Wan Kim, Kyung Tai Whang, Sung Hoon Cho
Clin Exp Pediatr. 1992;35(2):257-262.   Published online February 15, 1992
A narrow QRS paroxysmal supraventricular tachycardia is a common dysrrhythmia and medical emergency in childhood. We experienced a case of broad QRS type paroxysmal supraventricular tachycardia which was induced by transesophageal pacing technique and the morphology of the QRS complex was similar to that of ventricular tachycardia. So, We report this with a brief review and its related literatures.