Noun:

জন্মগত রোগ,

congenital disease শব্দের বাংলা অর্থ এর উদাহরণ:

বর্তমান আশকেনাজি ইহুদিগণ বিভিন্ন ধরনের জন্মগত রোগ এবং পরিব্যক্তিতে ভোগেন, যা অন্যান্য নৃগোষ্ঠীর তুলনায় আশকেনাজি ইহুদিদের ।

congenital disease's Usage Examples:

Birth defect Other names Congenital disorder, congenital disease, congenital deformity, congenital anomaly A boy with Down syndrome, one of the most common.

Although rare, the congenital disease is most prevalent among populations originating from China.

hemihyperplasia, or Friedreich's disease) abbreviated as (HFH) is rare congenital disease characterized by unilateral enlargement of the head and teeth.

Polysplenia is a congenital disease manifested by multiple small accessory spleens, rather than a single, full-sized, normal spleen.

Laryngomalacia is one of the most common laryngeal congenital disease in infancy and public education about the signs and symptoms of the.

Dyskeratosis congenita is congenital disease characterized by reticular skin pigmentation, nail degeneration, and.

"bullous acrokeratotic poikiloderma of Kindler and Weary",) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.

She was born with an extremely rare congenital disease called Marfanoid–progeroid–lipodystrophy syndrome that, among other.

Microcoria is a congenital disease in which the pupils of the subject are narrower than 2 mm in diameter.

referred as Nystagmus with congenital zonular cataract is a rare congenital disease associated with Nystagmus and zonular cataract of the eye.

It is a congenital disease and is also known as heterotopic, accessory, or aberrant pancreas.

Umbilical cord ulceration and intestinal atresia is a rare congenital disease that leads to intestinal atresia, umbilical cord ulceration and severe intrauterine.

The kidney: from normal development to congenital disease.

myopathy: is a congenital disease resulted from altered function of UDP-GlcNAc epimerase .

Macular corneal dystrophy: is a congenital disease resulted from.

significant progress in understanding, diagnosing and treating the congenital disease galactosemia.

with juvenile macular dystrophy (HJMD or CDH3) is an extremely rare congenital disease characterized by sparse hair growth (hypotrichosis) from birth and.

deteriorated in 1938, after his right leg was amputated due to a congenital disease.

She has a vision impairment because of a congenital disease.

Char syndrome is an autosomal dominant congenital disease caused by mutations in TFAP2B gene which affects the development of the bones of the face as.

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; genetic abnormality; maple syrup urine disease; Hirschsprung's disease; abetalipoproteinemia; congenital afibrinogenemia; genetic disorder; achondroplasia; hepatolenticular degeneration; 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;