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Chromosomal disorder with 4 X chromosomes
Tetrasomy X, also known as 48,XXXX or Poly-X Klinefelter, is a chromosomal disorder in which a female has four, rather than two, copies of the X chromosome
Tetrasomy_X
Chromosome disorder in women
trisomy X, some cases of tetrasomy X are mild, and some cases of trisomy X are severe. Like trisomy X, the full phenotypic range of tetrasomy X is unknown
Trisomy_X
Chromosomal disorder
as "coarse", much like those of the related disorder tetrasomy X. Pentasomy X is unique amongst X-chromosome polysomies for its association with short
Pentasomy_X
Medical condition
syndrome where partial tetrasomy of chromosome 22 is present Pallister-Killian syndrome (tetrasomy 12p) Tetrasomy 9p Tetrasomy 18p Tetrasomy 21, a rare form
Tetrasomy
Topics referred to by the same term
formation XXXX Derby, rugby league XXXX Gold Beach Cricket XXXX syndrome, Tetrasomy X, a chromosomal disorder XXXX Island, temporary promotional name given
XXXX
X chromosome monosomy
as 45,X, or 45,X0, is a chromosomal disorder in which cells of females have only one X chromosome instead of two, or are partially missing an X chromosome
Turner_syndrome
Index of articles associated with the same name
; Skakkebæk, Niels E.; Main, Katharina M.; Juul, Anders (2012-08-01). "45,X/46,XY Mosaicism: Phenotypic Characteristics, Growth, and Reproductive Function—A
Sex_chromosome_anomalies
Human chromosomal condition
46,XY/47,XYY, 48,XXYY, 49,XXXYY, 48,XXXX (known as tetrasomy X), and 49,XXXXX (known as pentasomy X). These medical conditions are considered intersex
XXYYY_syndrome
Chromosomal disorder
XXXYY and other high-level sex chromosome aneuploidies, such as tetrasomy X, pentasomy X, XYYY syndrome, XYYYY syndrome, and XXXXY syndrome, are survivable
XXXYY_syndrome
Sex chromosome present in both sexes in the XY and X0 sex-determination systems
condition. Females with more than one extra copy of the X chromosome (48, tetrasomy X or 49, pentasomy X) have been identified, but these conditions are rare
X_chromosome
Condition present at birth regardless of cause
Theriogenology, 15. https://doi.org/10.58292/ct.v15.9609 Chen, J; Gong, X; Chen, P; Luo, K; Zhang, X (16 August 2016). "Effect of L-arginine and sildenafil citrate
Birth_defect
Genetic disorder
Lancet (Review). 361 (9365): 1281–1289. doi:10.1016/S0140-6736(03)12987-X. PMID 12699967. S2CID 33257578. "Facts About Down Syndrome". National Association
Down_syndrome
Abnormal multiples of one or more chromosomes
tetrasomic inheritance, four copies of a linkage group rather than two (tetrasomy) assort two-by-two. Polysomy types are categorized based on the number
Polysomy
Natural premature termination of pregnancy
abnormalities found in miscarriages include an autosomal trisomy (22–32%), monosomy X (5–20%), triploidy (6–8%), tetraploidy (2–4%), or other structural chromosomal
Miscarriage
Extra X and Y chromosome in males
are more significantly affected. Sex chromosome anomalies Aneuploidy Tetrasomy X Taurodontism "48,XXYY syndrome | Genetic and Rare Diseases Information
XXYY_syndrome
Chromosomal disorder
chromosome aneuploidies such as XXXY syndrome and tetrasomy X—or indeed 49-chromosome disorders such as pentasomy X—are survivable with relatively mild phenotypes
XYYY_syndrome
Generalized neurodevelopmental disorder
rarest of cases, abnormalities with the X or Y chromosome may also cause disability. Tetrasomy X and pentasomy X syndrome affect a small number of girls
Intellectual_disability
Tetraamelia-syrinx Tetrahydrobiopterin deficiency Tetraploidy Tetrasomy 9p Tetrasomy 15qter syndrome Tetrasomy X Thakker–Donnai syndrome Thalamic degeneration symmetrical
List_of_diseases_(T)
Medical condition
Trisomy X (47,XXX) Tetrasomy X (48,XXXX) Pentasomy X (49,XXXXX) XYY syndrome (47,XYY) XYYY syndrome (48,XYYY) XYYYY syndrome (49,XYYYY) 45,X/46,XY 46
Fryns–Aftimos_syndrome
Medical condition
Literature". Adultspan Journal. 14 (1): 2–10. doi:10.1002/j.2161-0029.2015.00032.x. Christiansen, DM (February 2017). "Posttraumatic stress disorder in parents
Miscarriage and mental disorders
Miscarriage_and_mental_disorders
Biological process where inactive X chromosomes are reactivated
male breast cancer. In females, there is no evidence that trisomy X or tetrasomy X females are at higher risk of cancer. Breast cancer and ovarian cancer
X-chromosome_reactivation
Factors that increase the chance of a miscarriage
Endocrine Genetic and chromosome abnormalities Autosomal trisomy Monosomy X (45, X) Triploidy Structural abnormality of the chromosome Double or triple trisomy
Miscarriage_risks
Condition caused by four copies of the short arm of chromosome 12
The Pallister–Killian syndrome (PKS), also termed tetrasomy 12p mosaicism or the Pallister mosaic aneuploidy syndrome, is an extremely rare and severe
Pallister–Killian_syndrome
Human chromosomal condition
PMID 16650979. Linden MG, Bender BG, Robinson A (October 1995). "Sex chromosome tetrasomy and pentasomy". Pediatrics. 96 (4 Pt 1): 672–682. doi:10.1542/peds.96
Klinefelter_syndrome
Presence of an abnormal number of chromosomes in a cell
PMID 10215072. Linden MG, Bender BG, Robinson A (October 1995). "Sex chromosome tetrasomy and pentasomy". Pediatrics. 96 (4 Pt 1): 672–82. doi:10.1542/peds.96.4
Aneuploidy
Abnormal partial or mixed chromosome
syndrome: MedlinePlus Genetics". Xu H, Xiao B, Ji X, Hu Q, Chen Y, Qiu W (July 2014). "Nonmosaic tetrasomy 15q25.2 → qter identified with SNP microarray in
Small supernumerary marker chromosome
Small_supernumerary_marker_chromosome
for List of medical roots, suffixes and prefixes. Contents P Q R S T U V W X Y Z References Note that root groups such as "ad-, a-, ac-, af-, ag-, al-
List of Greek and Latin roots in English/P–Z
List_of_Greek_and_Latin_roots_in_English/P–Z
Rare chromosomal disorder
PMID 28137251. Linden MG, Bender BG, Robinson A (October 1995). "Sex chromosome tetrasomy and pentasomy". Pediatrics. 96 (4): 672–682. doi:10.1542/peds.96.4.672
XYYYY_syndrome
Condition caused by two joined and mirrored duplications of part of chromosome 15
Isodicentric 15, also called marker chromosome 15 syndrome, idic(15), partial tetrasomy 15q, or inverted duplication 15 (inv dup 15), is a chromosome abnormality
Isodicentric_15
1978 Australian film
Fantasy notes the similarity between the film's plot and that of the novel Tetrasomy Two by Oscar Rossiter (nom de plume of Dr. Vernon H.Skeels (1918-2007)
Patrick_(1978_film)
Rare genetic disease affecting palate, thumbs, and upper limbs
conditions Tetrasomy 18p Fitch N, Levy EP (1975). "Adducted thumb syndromes". Clin. Genet. 8 (3): 190–8. doi:10.1111/j.1399-0004.1975.tb01493.x. PMID 1175322
Adducted_thumb_syndrome
15, trisomy mosaicism Chromosome 15q, partial deletion Chromosome 15q, tetrasomy Chromosome 15q, trisomy Chromosome 16 – Chromosome 1q Chromosome 16, trisomy
List_of_diseases_(C)
DNA molecule containing genetic material of a cell
and overlapping fingers. Isodicentric 15, also called idic(15), partial tetrasomy 15q, or inverted duplication 15 (inv dup 15). Jacobsen syndrome, which
Chromosome
Human chromosome
disease type C Porphyria Selective mutism Edwards syndrome (trisomy 18) Tetrasomy 18p Monosomy 18p Pitt–Hopkins syndrome 18q21 Distal 18q- (distal deletion)
Chromosome_18
Birth defect of malformed rectum
anus are trisomies 18 and 21, the cat-eye syndrome (partial trisomy or tetrasomy of a maternally derived chromosome 22), Baller–Gerold syndrome, Currarino
Imperforate_anus
Tumor originating in adipose (fat) tissue
Ning S, Deng G, Xie Y, Song J, et al. (2020). "Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder"
Liposarcoma
beginning with other letters: A B C D E F G H I J K L M N O P Q R S T U V X Z σάκκος in Liddell and Scott σάκχαρ in Liddell and Scott σάλπιγξ in Liddell
List of Greek and Latin roots in English/S
List_of_Greek_and_Latin_roots_in_English/S
Electric current produced in living cells
Pavlina; Misovicova, Nadezda; Vrbicka, Dita (2013). "Partial trisomy and tetrasomy of chromosome 21 without down syndrome phenotype and short overview of
Developmental_bioelectricity
Abnormal small fragment of a chromosome
addition to the standard 46 chromosomes, making it a partial trisomy or tetrasomy supernumerary chromosome. A marker can be composed of inactive genetic
Marker_chromosome
chromosomes result in partial trisomy, and at other times, a partial tetrasomy. In partial tetrasomy, the karyotype appears normal except for the marker chromosome
Neocentromere
Medical condition
(601803), which is a dysmorphic syndrome with tissue-specific mosaicism of tetrasomy 12p. Veldman et al. (2002) discussed the differentiation between Fryns
Fryns_syndrome
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