| Health / Medical Topics |
Holoprosencephaly Type 1
The most severe form of holoprosencephaly in which there is a complete absence of midline forebrain division resulting in the presence of fused hemispheres and a single ventricle (alobar holoprosencephaly). It is mapped to chromosome 21q22. (NCI Thesaurus)
YOU MAY ALSO LIKE
A rare disorder characterized by the failure of the forebrain to divide into distinct hemispheres. It is associated with craniofacial abnormalities, developmental…
An epoch of the Quaternary period dating from the end of the Pleistocene approximately 11,000 years ago until the present. …
A rare autosomal recessive inherited disorder caused by mutations in the HLCS gene. It is characterized by deficiency of the enzyme holocarboxylase…
A radioactive isotope that is used to destroy cancer cells.
Holmium Ho166 containing poly l-lactic acid (PLA) microspheres with potential antineoplastic actvity. Upon intra-arterial hepatic administration of holmium 166 microspheres, this agent…
A drug containing a radioactive isotope that is used in the diagnosis and treatment of cancer.
