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1.
J Pak Med Assoc ; 72(9): 1838-1841, 2022 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-36280987

RESUMEN

The objective of this study was to determine the frequency and outcome of preterm infants diagnosed with Necrotising Enterocolitis (NEC). In a case series, 320 preterm infants were enrolled during a period of 12 months at Aga Khan University Hospital, Karachi, a tertiary care hospital. Diagnosis and staging was done as per Bell's staging criteria. Possible confounders were filtered. Analysis was based on the form of treatment and symptom progression. During the study, NEC was observed in 29(9.06%) babies of which stages I, II and III were 69%, 24% and 7%, respectively. Outcome analysis showed that among the 29 neonates diagnosed with NEC, 23 were discharged and 6 expired. A 9% prevalence observed during the study suggests this to be to be a major challenge in neonatology. Mortality outcome of 21% diagnosed with NEC recommends an early diagnosis coupled with prompt and appropriate treatment and preventive measures to reduce the burden of NEC in future.


Asunto(s)
Enterocolitis Necrotizante , Enfermedades del Recién Nacido , Lactante , Recién Nacido , Humanos , Enterocolitis Necrotizante/diagnóstico , Enterocolitis Necrotizante/epidemiología , Enterocolitis Necrotizante/terapia , Recien Nacido Prematuro , Diagnóstico Precoz , Hospitales
2.
J Pak Med Assoc ; 72(5): 975-977, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-35713069

RESUMEN

Fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO syndrome) is a rare, genetic, congenital limb malformation characterised by unilateral or bilateral fibular aplasia, tibial campomelia, and lower limb oligosyndactyly involving the lateral rays. A newborn male born at term via a Caesarean Section presented with malformations consisting of tibial campomelia, unilateral fibular hypoplasia, and oligosyndactyly, a "FATCO variant" case. On radiographic examination, an anterolateral shortened and bowed right lower limb at the distal third of the tibia, a rudimentary right fibula and absence of three rays on right foot were revealed. "FATCO syndrome" although rare may be linked to involvement of different body systems with morbidity and mortality. Proper parent counseling is a key aspect of this syndrome. Timely diagnosis and management with a multidisciplinary approach is essential to avoid lifelong disability, which can be a hurdle in a developing country.


Asunto(s)
Displasia Campomélica , Sindactilia , Displasia Campomélica/diagnóstico , Displasia Campomélica/terapia , Cesárea , Femenino , Peroné/anomalías , Peroné/diagnóstico por imagen , Dedos/anomalías , Deformidades Congénitas del Pie , Deformidades Congénitas de la Mano , Humanos , Lactante , Recién Nacido , Masculino , Embarazo , Sindactilia/diagnóstico , Sindactilia/genética , Síndrome , Tibia/anomalías , Tibia/diagnóstico por imagen , Dedos del Pie/anomalías
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