Deficiency of " CTSD " gene has been reported an underlying cause of neuronal ceroid lipofuscinosis ( NCL ).
12.
Mutations in the " TPP1 " gene lead to late infantile neuronal ceroid lipofuscinosis, a fatal neurodegenerative disease of childhood.
13.
Mutations in this gene are associated with progressive epilepsy with mental retardation ( EPMR ), a subtype of neuronal ceroid lipofuscinosis ( NCL ).
14.
Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 ( CLN1, or INCL ) and neuronal ceroid lipofuscinosis 4 ( CLN4 ).
15.
Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 ( CLN1, or INCL ) and neuronal ceroid lipofuscinosis 4 ( CLN4 ).
16.
The neuronal ceroid lipofuscinoses ( NCLs ) are a group of inherited neurodegenerative disorders with pathological phenotypes that auto fluorescent lipopigments present in neurons and other cell types.
17.
The luminal cells will often have decapitation ( apocrine ) secretions and will also have yellow-brown, ceroid, lipofuscin-like ( cerumen ) pigment granules.
18.
"' Jansky Bielschowsky disease "'is an extremely rare autosomal recessive genetic disorder that is part of the neuronal ceroid lipofuscinosis ( NCL ) family of neurodegenerative disorders.
19.
Mutations of gene " TPP1 " result in late-infantile neuronal ceroid lipofuscinosis which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome.
20.
In 2 Mexican siblings with infantile onset of progressive myoclonic epilepsy and pathologic findings of neuronal ceroid lipofuscinosis in multiple cell types, a homozygous mutation in the KCTD7 gene ( R184C ) has been identified.
How to say ceroid in Hindi and what is the meaning of ceroid in Hindi? ceroid Hindi meaning, translation, pronunciation, synonyms and example sentences are provided by Hindlish.com.
