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1.
Journal of the Korean Pediatric Society ; : 1717-1724, 1999.
Artículo en Coreano | WPRIM | ID: wpr-143053

RESUMEN

PURPOSE: Congenital adrenal hyperplasia(CAH), which is classified into salt-wasting, simple virilization and non-classic type according to clinical features, is difficult to detect in early stages. Failure to diagnose it in the initial state may lead to life-threatening adrenal crisis, inappropriate male sex assignment in the genetic female, acceleration of skeletal maturation and subsequent short stature. Therefore, we studied the variables increasing the 17-hydroxyprogesterone(OHP) values for more specific and sensitive diagnosis of CAH. METHODS: We classified 3,532 newborns into variable factors; gestational age, birth weight, gender, delivery type, sampling date and stress. Then, we analysed the relationships between 17-OHP values and variable factors. RESULTS: The mean value of 17-OHP was 4.21+/-0.03ng/ml. There were significant differences among the variable factors except gender. The mean value of male was 4.26ng/ml, and that of female was 4.15ng/ml(P=0.10). The mean value of 17-OHP in vaginal delivered newborn was higher than C-section delivered ones(4.71ng/ml, 3.34ng/ml, P=0.0001). It was also higher in low birth weight(P=0.0001), in prematurity(P=0.001), those sampled within 4 days(P=0.0001), stressful condition and ventilator care-assisted(P=0.004). CONCLUSION: 17-OHP value in neonatal screening is influenced by several variables such as vaginal delivery, ventilator management, low birth weight, sampling date and prematurity. If the 17-OHP value is increased, we have to consider the variables influencing the increase in value and follow up with time interval or analysis of genetic mutations.


Asunto(s)
Femenino , Humanos , Recién Nacido , Masculino , 17-alfa-Hidroxiprogesterona , Aceleración , Hiperplasia Suprarrenal Congénita , Peso al Nacer , Diagnóstico , Estudios de Seguimiento , Edad Gestacional , Recién Nacido de Bajo Peso , Tamizaje Masivo , Tamizaje Neonatal , Parto , Ventiladores Mecánicos , Virilismo
2.
Journal of the Korean Pediatric Society ; : 1717-1724, 1999.
Artículo en Coreano | WPRIM | ID: wpr-143048

RESUMEN

PURPOSE: Congenital adrenal hyperplasia(CAH), which is classified into salt-wasting, simple virilization and non-classic type according to clinical features, is difficult to detect in early stages. Failure to diagnose it in the initial state may lead to life-threatening adrenal crisis, inappropriate male sex assignment in the genetic female, acceleration of skeletal maturation and subsequent short stature. Therefore, we studied the variables increasing the 17-hydroxyprogesterone(OHP) values for more specific and sensitive diagnosis of CAH. METHODS: We classified 3,532 newborns into variable factors; gestational age, birth weight, gender, delivery type, sampling date and stress. Then, we analysed the relationships between 17-OHP values and variable factors. RESULTS: The mean value of 17-OHP was 4.21+/-0.03ng/ml. There were significant differences among the variable factors except gender. The mean value of male was 4.26ng/ml, and that of female was 4.15ng/ml(P=0.10). The mean value of 17-OHP in vaginal delivered newborn was higher than C-section delivered ones(4.71ng/ml, 3.34ng/ml, P=0.0001). It was also higher in low birth weight(P=0.0001), in prematurity(P=0.001), those sampled within 4 days(P=0.0001), stressful condition and ventilator care-assisted(P=0.004). CONCLUSION: 17-OHP value in neonatal screening is influenced by several variables such as vaginal delivery, ventilator management, low birth weight, sampling date and prematurity. If the 17-OHP value is increased, we have to consider the variables influencing the increase in value and follow up with time interval or analysis of genetic mutations.


Asunto(s)
Femenino , Humanos , Recién Nacido , Masculino , 17-alfa-Hidroxiprogesterona , Aceleración , Hiperplasia Suprarrenal Congénita , Peso al Nacer , Diagnóstico , Estudios de Seguimiento , Edad Gestacional , Recién Nacido de Bajo Peso , Tamizaje Masivo , Tamizaje Neonatal , Parto , Ventiladores Mecánicos , Virilismo
3.
Journal of Korean Society of Pediatric Endocrinology ; : 127-132, 1997.
Artículo en Inglés | WPRIM | ID: wpr-156788

RESUMEN

We report an extremely specific case of Pendred's syndrome, originally described with an association of thyroid organification defect and hearing impairment; normal-sized thyroid, severe hypothyroidism manifested by profoundly retarded physical and mental development, cardiomegaly and severe hypochromic & microcytic anemia associated with asymmetrical septal hypertrophy.


Asunto(s)
Adolescente , Humanos , Anemia , Cardiomegalia , Pérdida Auditiva , Hipertrofia , Hipotiroidismo , Glándula Tiroides
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