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1.
Korean Journal of Pediatrics ; : 1287-1292, 2004.
Article in Korean | WPRIM | ID: wpr-46071

ABSTRACT

PURPOSE: To test the usefulness of a new jaundice meter, the JM-103(Minolta/Hill-Rom Air-shields, Japan) which uses a new probe to compensate for different skin pigmentation or thickness, and displayed actual bilirubin level instead of an index number as in the previous model, the JM-102, we compared transcutaneous bilirubin(TCB) with plasma bilirubin(PB) in newborn infants. METHODS: TCB was measured on 114 newborn infants aged 3 to 6 days with jaundice meter JM- 103, using one to five flashes. TCB was measured on the forehead(glabella; TCB-F) and on the chest(sternum; TCB-C) of the same infant at the same time. PB was measured by American Optical bilirubinometer within 30 minutes after TCB measurement. TCB was compared with PB, and the difference of TCB according to the using preset numbers of flashing times was studied. RESULTS: There was significant correlation between PB and TCB, regardless of the measuring site and the numbers of flashing during measurement. CONCLUSION: The New transcutaneous bilirubinometer, the JM-103 would be a useful screening device in neonatal jaundice.


Subject(s)
Humans , Infant , Infant, Newborn , Bilirubin , Jaundice , Jaundice, Neonatal , Mass Screening , Plasma , Skin Pigmentation
2.
Journal of the Korean Society of Neonatology ; : 236-240, 2004.
Article in Korean | WPRIM | ID: wpr-15026

ABSTRACT

Congenital cytomegalovirus (CMV) infection is one of the most frequent congenital infections in neonates. It can manifest as asymptomatic infection in 90% or symptoms may appear in 10% of the patients. Asymptomatic congenital CMV infection is likely to be a leading cause of sensorineural hearing loss, mental retardation and microcephaly. Incontinentia pigmenti is a rare multisystemic ectodermal disorder, which is characterized by vesicular, verrucous, and pigmented cutaneous lesions, and is frequently associated with various developmental defects of the eyes, CNS, teeth, hair, and nail. It is regarded as an X-linked dominent genetic disorder. We are reporting a case of neonate who presented with delayed development and bilateral hearing loss due congenital CMV infection which was incidentally assoicated with incontinentia pigmenti.


Subject(s)
Humans , Infant, Newborn , Asymptomatic Infections , Cytomegalovirus , Ectoderm , Hair , Hearing Loss , Hearing Loss, Bilateral , Hearing Loss, Sensorineural , Incontinentia Pigmenti , Intellectual Disability , Microcephaly , Tooth
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