Noun:

জিনগত অস্বাভাবিকতা,

genetic abnormality শব্দের বাংলা অর্থ এর উদাহরণ:

আফ্রিকাবাসীদের এক সাধারণ জিনগত অস্বাভাবিকতা, যাকে বলে গ্লুকোজ-6-ফসফেট ডিহাইড্রোজেনাস ডেফিসিয়েন্সি, বিপদকে বাড়িয়ে ।

genetic abnormality's Usage Examples:

X-chromosomes, while males only have a single X chromosome, and a genetic abnormality located on the X chromosome is much more likely to cause clinical.

adjacent teeth, dense overlying bone, excessive soft tissue or a genetic abnormality.

significant differences in clinical severity among relatives with the same genetic abnormality at the MTM1 gene.

woman of exceptional stature, often the result of some medical or genetic abnormality (see gigantism).

This genetic abnormality can result in the birth of a normal child who has no obvious disability.

Philadelphia chromosome or Philadelphia translocation (Ph) is a specific genetic abnormality in chromosome 22 of leukemia cancer cells (particularly chronic myeloid.

Huntington's disease, a neurodegenerative illness which is the result of a genetic abnormality, whose symptoms typically appear in mid-life.

This discovery was the first association between a genetic abnormality and a type of cancer, and it changed the direction of cancer research.

- Means Latin for 'freak of nature' and refers to a woman with a genetic abnormality and who is mistaken for a vampire.

researcher David Hungerford is credited with the discovery of the first genetic abnormality in cancer, called the Philadelphia chromosome.

Two to 5% of women with POI and a premutation in FMR1, a genetic abnormality, are at risk of having a child with fragile X syndrome, the most.

Cleidocranial dysostosis (also called cleidocranial dysplasia), a genetic abnormality in humans Central core disease, a rare neuromuscular disorder Congenital.

A natural freak would usually have been born with a genetic abnormality, while a made freak was a person who had an artificial alteration.

each are classified from both the altered lipid profile and by the genetic abnormality.

autosomal recessive condition called Naxos disease, because this genetic abnormality can also affect the integrity of the superficial layers of the skin.

Williams syndrome is caused by a genetic abnormality, specifically a deletion of about 27 genes from the long arm of one.

While there is no treatment to correct the genetic abnormality of this syndrome, there is the potential to treat the symptoms.

solitary, and is a neoplasm resulting from a genetic mutation (or other genetic abnormality) in a single precursor cell.

The genetic abnormality occurs randomly in sperm or egg cells or it may occur in early embryonic.

Synonyms:

branched chain ketoaciduria; achondroplasty; McArdle's disease; oligodactyly; marble bones disease; inborn error of metabolism; Fanconi's anemia; dwarfism; osteopetrosis; lactose intolerance; polygenic disorder; inherited disease; mucopolysaccharidosis; autosomal dominant disease; congenital megacolon; Albers-Schonberg disease; genetic defect; nanism; maple syrup urine disease; Hirschsprung's disease; abetalipoproteinemia; congenital afibrinogenemia; genetic disorder; achondroplasia; hepatolenticular degeneration; congenital disease; Wilson's disease; hereditary condition; Spielmeyer-Vogt disease; juvenile amaurotic idiocy; dystrophy; milk intolerance; monogenic disease; porphyria; oligodontia; hyperbetalipoproteinemia; otosclerosis; osteosclerosis congenita; polygenic disease; Fanconi's anaemia; congenital pancytopenia; autosomal recessive disease; pachyderma; hereditary disease; chondrodystrophy; autosomal recessive defect; lactase deficiency; autosomal dominant disorder; monogenic disorder; inherited disorder; genetic disease; nevoid elephantiasis; muscular dystrophy; ichthyosis; disease;

Antonyms:

wellness;