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Article | IMSEAR | ID: sea-185167

ABSTRACT

Late onset HDN can present as bleeding from any site of the body but more commonly from intracranial vessels. It is diagnosed if bleeding occurs after 7th day of life with normal platelet count, prolonged prothrombin time (PT) and activated partial thromboplastin time (aPTT), associated with stopping of bleeding and PT/PTTreturning to normal after giving vitamin K. Among the types of intracranial bleeding in late hemorrhagic disease of newborn, intracerebral parenchymal bleeding is least common.

2.
Indian Pediatr ; 2014 Aug; 51(8): 608-610
Article in English | IMSEAR | ID: sea-170717
3.
Indian J Hum Genet ; 2011 Jan; 17(1): 26-28
Article in English | IMSEAR | ID: sea-138928

ABSTRACT

Ectrodactyly, ectodermal dysplasia and cleft palate syndrome is a rare autosomal dominant multiple congenital anomaly syndrome with variable expressivity and reduced penetration. The cardinal features are cleft palate/lip, lobster hand deformity, sparse hypopigmented hair, dry scaly skin, and lacrimal and urogenital anomalies. A neonate presented to us with typical features, his mother and other two siblings were also affected.


Subject(s)
Abnormalities, Multiple/etiology , Adult , Child , Cleft Lip/epidemiology , Cleft Lip/genetics , Cleft Palate/epidemiology , Cleft Palate/genetics , Cluster Analysis , Ectodermal Dysplasia/epidemiology , /genetics , Foot Deformities, Congenital/epidemiology , Foot Deformities, Congenital/genetics , Hand Deformities, Congenital/epidemiology , Hand Deformities, Congenital/genetics , Fingers/abnormalities , Hair Color , Humans , Ichthyosis/etiology , Infant, Newborn , Lacrimal Apparatus/abnormalities , Pigmentation Disorders/etiology , Siblings , Syndrome , Urogenital Abnormalities/etiology
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