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Trisomy in Medical Dictionary

Translocation

... three # 21 chromosomes , just like there are in trisomy 21, but one of the 21 chromosomes is attached ... breaks off and s ticks to another chromosome . trisomy The condition of having three identical ... after birth . Chromosome studies show trisomy 13 , partial ...

Trisomy 13

... trisomy 13 syndrome : Condition with three rather than ... due to the extra chromosome #13. trisomy 13 can be diagnose d prenatal ly by ... with chromosome studies of the amniotic cells. trisomy 13 mosaicism and partial ...

Trisomy

... trisomy 18 and trisomy 13 are genetic disorders that present a ... nearly every organ system in the body. trisomy 13 syndrome : Condition with three rather than ...

Trisomy 18

... trisomy 18 and trisomy 13 are genetic disorders that present a ... nearly every organ system in the body. trisomy 18 syndrome : There are three instead of the ...

Amniocentesis

... is called amniocentesis . All of these findings are secondary to trisomy (an extra chromosome ) of the 21st chromosome . trisomy 21 can be detected in the first few months of pregnancy by ...

Chromosome

... to the usual pair. Down syndrome is an example of a condition caused by trisomy . truss A device to keep a hernia in its proper place. Labor atory ... presence of a suspected disorder. Disclaimer: ... CAUSES"Also called trisomy 21, Down syndrome occurs during fetal development , but is not ...

Cleft lip and palate

... made an exceptional difference in our lives. Patau syndrome ( trisomy 13 syndrome ): A syndrome characterized by multi ple malformations, ... Cryotherapy Cystoscopy in the Urology Clinic ... Babies with trisomy 18 may also have spina bifida (in 6 percent of cases), eye problems ...

Noonan syndrome

... congenital heart disease (not all cyanotic) are Down syndrome , trisomy 13 , Turner's syndrome , Marfan syndrome , Noonan syndrome , and Ellis ... various genetic and chromosomal syndrome s, such as Down syndrome , trisomy 13 , Turner's syndrome , Marfan syndrome , Noonan syndrome , ... ...

Velo-Cardio-Facial Syndrome

... from very mild to severe. In this article What is it? Down syndrome trisomy 18 and trisomy 13 Turner's syndrome Cri du chat syndrome Wolf-Hirshhorn syndrome ...

Acute lymphocytic leukemia

... include heart defects, esophageal atresia , and an increased incidence of acute lymphocytic leukemia . All of these findings are secondary to trisomy (an extra chromosome ) of the 21st chromosome . Additional phase I/II trials have begun to evaluate the efficacy of annamycin in the treatment ...

Atresia

... heart defects, esophageal atresia , and an increased incidence of acute lymphocytic leukemia . All of these findings are secondary to trisomy (an extra chromosome ) of the 21st chromosome . In biliary atresia , the bile ducts are actually absent, also causing jaundice . Cancer ...

Chromosomes

... attached to the 21st of the 23 pairs of chromosomes normally present in the human genome. This third chromosome gives rise to the alternate name trisomy 21. their bodies have not experienced the normal puberty -related rise in body fat that triggers the beginning of menstruation . In other ...

Cleft lip

... 10,000 IU daily. Excessive intake of vitamin A is linked to cleft palate , heart defects, and other congenital defects. Patau syndrome ( trisomy 13 syndrome ): A syndrome characterized by multi ple malformations, commonly including scalp defects, hemangioma s ( blood vessel ...

Esophageal atresia

... include heart defects, esophageal atresia , and an increased incidence of acute lymphocytic leukemia . All of these findings are secondary to trisomy (an extra chromosome ) of the 21st chromosome . Occasionally, early feeding problems are due to anatomical difficulties (for example, a ...

Fetal development

... defects form during fetal development and may result in abnormal blood flow through the heart after a baby is born. CAUSES"Also called trisomy 21, Down syndrome occurs during fetal development , but is not inherited. The problem is an extra 21st chromosome . It occurs in 1 out of 700 ...

Hurler syndrome

... the disease . Hurler syndrome Waardenburg syndrome Kartagener syndrome Fronto-metaphyseal dysplasia syndrome Morquio syndrome trisomy 13 S Multi ple lentigines syndrome Treacher Collins syndrome Stickler syndrome ... peyer's; peyer's glands ; peyer's patch; Peyer's ...

Morquio syndrome

... mycosis ... Hurler syndrome Waardenburg syndrome Kartagener syndrome Fronto-metaphyseal dysplasia syndrome Morquio syndrome trisomy 13 S Multi ple lentigines syndrome Treacher Collins syndrome Stickler syndrome ... ...

Palate

... . The pharynx is a tube that connects the mouth and nasal passages with the esophagus , the connection to the stomach . Patau syndrome ( trisomy 13 syndrome ): A syndrome characterized by multi ple malformations, commonly including scalp defects, hemangioma s ( blood vessel ...

Simian crease

... have three creases in their palms. Simian crease : A single transverse palmar crease, a minor variation associated with Down syndrome ( trisomy 21). Also called a four-finger crease, single palmar flexion crease, single upper palm crease, or line. Sibilant Rhonchi ( Wheezing ) Side Pain ...

Treacher

... Disorder ) ... Hurler syndrome Waardenburg syndrome Kartagener syndrome Fronto-metaphyseal dysplasia syndrome Morquio syndrome trisomy 13 S Multi ple lentigines syndrome Treacher Collins syndrome Stickler syndrome ... ...

Waardenburg syndrome

... syndrome . Hurler syndrome Waardenburg syndrome Kartagener syndrome Fronto-metaphyseal dysplasia syndrome Morquio syndrome trisomy 13 S Multi ple lentigines syndrome Treacher Collins syndrome Stickler syndrome ... ...
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