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1.
Indian Pediatr ; 2013 May; 50(5): 463-467
Artículo en Inglés | IMSEAR | ID: sea-169801

RESUMEN

Objective: To develop and validate a simple screening tool which can be used in the Community to identify delay in language development among children of 0-3 years of age. Methods: The normal range for the 33-items of “Language Evaluation Scale Trivandrum for 0-3years-LEST(0-3)” were carefully selected from various existing language development charts and scales, by experts keeping in mind the face validity and content validity. The criterion validity was assessed using a community sample of 643 children of 0 to 3 years of age, including 340 (52.9%) boys. LEST (0-3) was validated against Receptive Expressive Energent Language Scale, for screening delay in language development among children of 0-3 years. Results: When one item delay was taken as ‘LEST delay’ (test positive), the sensitivity and specificity of LEST(0-3), was found to be 95.85% and 77.5%, respectively with a negative predictive value of 99.8% and LR (negative) of 0.05.When two item delay was taken as ‘LEST delay’ (test positive), the sensitivity and specificity of LEST(0-3), was found to be 66.7% and 94.8% respectively with a negative predictive value of 98.7% and LR (negative) of 0.35. The test-retest and inter-rater reliability were good and acceptable (Inter-class correlation of 0.69 for testretest and 0.94 for inter-rater). Conclusion: LEST (0-3) is a simple, reliable and valid screening tool for use in the community to identify children between 0-3 years with delay in language development, enabling early intervention practices.

2.
Indian J Pediatr ; 2009 Feb; 76(2): 151-5
Artículo en Inglés | IMSEAR | ID: sea-81611

RESUMEN

OBJECTIVE: To define the clinical manifestations of Chikungunya infection in infants. METHODS: The inclusion criteria was fever (defined as axillary temperature > 99.6 degrees F) with any one of the following features; seizure, loose stools, peripheral cyanosis, skin manifestations or pedal edema in children less than one year. Details of disease from onset of illness till admission were noted and a thorough clinical examination was done at the time of admission. Daily follow-up was performed and the serial order of appearance of clinical features was noted till complete recovery. The sera collected from patients after the 7th day of onset of fever was analyzed for specific chikungunya antibody by IgM antibody capture enzyme linked immunosorbent assay (ELISA). RESULTS: Fifty six (56) infants were laboratory confirmed for chikungunya, consisting of 34 (60.71%) males and 22 (39.29%) females. 4 (7.14%) infants were less than 1 month of age, 39 (69.64%) 2-6 months old and 13 (23.21%) 7-12 months old. Fever was invariably present, but associated constitutional symptoms in infants consisted of lethargy or irritability and excessive cry. The most characteristic feature of the infection in infants was acrocyanosis and symmetrical superficial vesicobullous lesions were noted in most infants. Erythematous asymmetrical macules and patches were observed which later progressed to morbiliform rashes. The face and oral cavity was spared in all observed patients. CONCLUSION: An entirely different spectrum of disease is seen in infants with chikungunya as compared to older children who need to be carefully observed for. The morbidity and mortality of the disease may be avoided by the rational use of drugs and close monitoring of all infants.


Asunto(s)
Infecciones por Alphavirus/diagnóstico , Infecciones por Alphavirus/inmunología , Virus Chikungunya/aislamiento & purificación , Ensayo de Inmunoadsorción Enzimática , Femenino , Humanos , Inmunoglobulina M , Lactante , Recién Nacido , Masculino , Enfermedades de la Piel/diagnóstico , Enfermedades de la Piel/inmunología
3.
Indian J Pediatr ; 2007 Oct; 74(10): 947-9
Artículo en Inglés | IMSEAR | ID: sea-79432

RESUMEN

Permanent neonatal diabetes mellitus (PNDM) is characterized by the onset of diabetes within the first six months of life and insulin dependence life long. It has been recently discovered that mutation in KCNJ11 gene encoding Kir6.2, the pore forming subunit of ATP sensitive potassium channel (K ATP) is the most common cause and such patients may respond better to oral sulphonylurea drugs than insulin. Here is a rare case of permanent neonatal diabetes due to R20IC mutation in KCNJ11 gene.


Asunto(s)
Sustitución de Aminoácidos/genética , Arginina/genética , Glucemia/metabolismo , Cisteína/genética , Análisis Mutacional de ADN , Diabetes Mellitus Tipo 1/diagnóstico , Cetoacidosis Diabética/sangre , Femenino , Gliburida/administración & dosificación , Tamización de Portadores Genéticos , Humanos , Hipoglucemiantes/administración & dosificación , Lactante , Recién Nacido , Insulina/administración & dosificación , Lesión Renal Aguda/sangre , Canales de Potasio de Rectificación Interna/genética
4.
Indian J Pediatr ; 2002 Nov; 69(11): 1003-5
Artículo en Inglés | IMSEAR | ID: sea-81576

RESUMEN

Bacillary angiomatosis is characterized by unique vascular lesions caused by infection with a small Gram staining bacillus of the genus Bartonella. It usually occurs in immunocompromised persons but can also occur in immunocompetent persons. We report a case of cutaneous bacillary angiomatosis in a 5-year-old immunocompetent child. He had infected lesions on the lips, after an injury, which was followed by lesions over the knees, buttocks, near the ankles and the elbows. Diagnosis was proved on histology. The lesions cleared after administration of erythromycin for 3 months. It is well to be aware of this condition in the context of increasing prevalence of AIDS.


Asunto(s)
Angiomatosis Bacilar/diagnóstico , Antibacterianos/uso terapéutico , Preescolar , Eritromicina/uso terapéutico , Humanos , Masculino
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