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1.
Indian J Pediatr ; 2006 May; 73(5): 439-40
Artículo en Inglés | IMSEAR | ID: sea-80885

RESUMEN

Noma Neonatorum is characterized by a gangrenous process involving mucocutaneous junctions of oral, nasal and anal area and occasionally, the eyelids and scrotum. It is seen during the first few weeks of neonatal life in premature and low birth weight babies. Noma Neonatorum is commonly described with pseudomonas aeruginosa septicemia. A case of Noma Neonatorum associated with E.coli sepsis is described for the first time.


Asunto(s)
Infecciones por Acinetobacter/complicaciones , Infecciones por Escherichia coli/complicaciones , Resultado Fatal , Humanos , Recién Nacido , Masculino , Noma/microbiología , Sepsis/microbiología
2.
Indian J Pediatr ; 2005 Apr; 72(4): 367
Artículo en Inglés | IMSEAR | ID: sea-79226

RESUMEN

Sirenomelia is an exceptionally rare congenital malformation characterized by complete or near complete fusion of lower limbs. A newborn with clinical features of sirenomelia including fused lower limbs in medial position, absent fibula, anal atresia, complete absence of urogenital system (bilateral renal agenesis, absent ureters, urinary bladder, absent internal and external genitalia), a single umbilical artery and a vestigial tail is reported. Association of vestigial tail with sirenomelia is not described in the literature.


Asunto(s)
Autopsia , Cóccix/anomalías , Ectromelia/complicaciones , Femenino , Humanos , Recién Nacido
3.
Indian Pediatr ; 2005 Mar; 42(3): 285-7
Artículo en Inglés | IMSEAR | ID: sea-13526

RESUMEN

Fanconi's anemia (FA) is a paradigm for congenital anomalies, aplastic anemia and predisposition to malignancies. Identification of the disease at birth is based on characteristic physical malformations, as hematologic manifestations at birth are extremely rare. We report a case of FA in a newborn who presented with anophthalmia, unilateral radial ray defect, hemivertebrae and thrombocytopenia.


Asunto(s)
Anomalías Múltiples/genética , Anoftalmos/genética , Anemia de Fanconi/diagnóstico , Humanos , Recién Nacido , Masculino , Trombocitopenia/genética
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