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Migraine in children

Migraine headaches in children are common and are usually not serious, presenting as severe chronic daily headaches or stress related headaches...
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Giant Cell Disease of the Liver

It is the liver injury in new borns inwhom the infectious and metabolic disease have been excluded. It is also called as idiopathic neonatal hepatitis...
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Absence Defect of Limbs Scalp and Skull

Absence Defect of Limbs Scalp and Skull or Adams Oliver Syndrome is also known as Congenital Scalp Defects with Distal Limb Reduction Anomalies or...
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Nanocephalic Dwarfism

Nanocephalic dwarfism or Seckel syndrome is a rare inherited disorder characterised mainly by retarded growth, mental retardation, small head and a...
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ACADM Deficiency

ACADM is a gene which if mutated may lead to Medium chain Acyl coenzyme- A dehydrogenase deficiency (MCAD). The condition is also referred as MCAD...
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Acrodermatitis Enteropathica

Acrodermatitis enteropathica (AE) is an autosomal recessive disorder, metabolic disorder affecting the uptake of zinc, characterized by...
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Aase Syndrome or Aase smith syndrome

It is a rare inherited disorder charecterized by anemia withjoint and skeletal deformities. It is an autosomal dominant inherited disorder. The...
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Ataxia Telangiectasia

Ataxia-telangiectasia (A-T) is an autosomal recessive, complex, multisystem disorder characterized by progressive neurologic impairment, cerebellar ataxia...
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Zinsser Cole Engman Syndrome

Zinsser Cole Engman Syndrome is also known as Cole's syndrome, Cole Rauschkolb Toomey syndrome, Hoyeraal Hreidarsson Syndrome, Zinsser's syndrome,...
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Aase Smith Syndrome II

It is a genetic disorder charecterized by presence of three bones with in the thumbs and reduced production og the red blood cells leading to...
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