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Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.
- Al-Kouatly H B, Chasen S T, Gilbert F, Ahner R, Alonso L M, Chervenak F A.: Correlation between rare chromosomal abnormalities and prenatal ultrasound findings. AJMG 10.1002/ajmg.10130;107:197-200, 2002. [PubMed: 11807899]Case No. 1=46,XX,inv(1)(p22q32)de novoMother was 36 years old. Hemivertebra was noted at ultrasound. Congenital kyphosis with normal renal ultrasound was the outcome.Aberration: Inversion pericentricIndex Terms: Hemivertebra
- Boue A, Gallano P: A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses. Prenat. Diag. 4:45-67, 1984. [PubMed: 6463033]t(1;9)(p22;p23); t(1;10)(p36;q24).Aberration: Reciprocal translocationNegative band
- Bovicelli L, Orgini L F, Rizzo N, Montacuti V, Bachetta M: "Prenatal diagnosis of a de novo reciprocal translocation 46,XX,t(1;18)(p22;q23)." Clin. Genet. 18:434-435, 1980. [PubMed: 7449182]"The parents......decided to terminate the pregnancy". The aborted fetus showed no malformations.Aberration: Reciprocal translocationNegative band
- Byrd J R, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]Observation No. 2546,XX,t(1;4)(p22;q35)mat.Aberration: Reciprocal translocationNegative band
- Carroll A J, Prchal J T, Finley W H: Transient hematologic disturbance in three members of a family segregating a balanced chromosome translocation. AJHG 36:265(Abstract), 1984.
Yang-Feng T L, Bruns G, Carroll A J, Simola K O J, Francke U: Localization of the LDHA gene to 11p14 to 11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13. Hum. Genet. 74:331-334, 1986. [PubMed: 3793094]Aberration: Simple translocationNegative band - Chitayat D, Fagerstrom C L, Kalousek D K, Rootman J, Taylor G P, Hall J G: "De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome." AJMG 32:36-41, 1989. [PubMed: 2495721]Patinet B.T.46,XY,t(1;2)(p22;q22).Some of the features were growth failure, mental retardation, microcephaly, cryptorchidism, partial syndactyly of the second and third toes and an unusual facial appearance.Aberration: Reciprocal translocationMIM#: 270400Negative band
- de Michelena M I, Villacorta J, Chavez J: "Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21)." AJMG 36:29-32, 1990. [PubMed: 2185634]46,XX,t(1;11)del(5)(pter -> q15::q31 -> qter)de novo.Aberration: Reciprocal translocationChromosomal Aneuploidy: 5q-Negative band
- Deroover J, Fryns J P, Haegeman J, van den Berghe H: Paracentric inversion in the short arm of chromosome 1. Hum. Genet. 49:117-121, 1979. [PubMed: 468242]
Fryns J P, van den Berghe H: Paracentric inversion in man: personal experience and review of literature. Hum. Genet. 54:413-416, 1980. [PubMed: 7399530]Family V.D.C.46,XX,inv(1)(p22p36).Patient MV, 19 years old was an anxious, autistic, severely retarded girl.46,XY,inv(1)(p22p36).&46,XY,inv(1)(pter -> p36::p22 -> p36::p22 -> qter).Aberration: Inversion paracentricNegative band - Dhadial R K, Smith M F: "Terminal 7p deletion and 1;7 translocation associated with craniosynostosis." Hum. Genet. 50:285-289, 1979. [PubMed: 489013]46,XX,t(1;7)(p22;p15),del(7)(pter -> p15).Parental karyotypes were normal.Aberration: Simple translocationMIM#: 218500Index Terms: CraniosynostosisNegative band
- Diedrich U, Hansmann I, Janke D, Opitz O, Probeck H D: Chromosome anomalies in 136 couples with a history of recurrent abortions. Hum. Genet. 65:48-52, 1983. [PubMed: 6642507]46,XX,rcp(1;8)(p22;q22).Aberration: Reciprocal translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)Negative band
- Donahue S P, Wenger S L, Steele M W, Gorin M B.: Broad-spectrum Mobius syndrome associated with a 1;11 chromosome translocation. Ophthal. Paediat. Genet. 14:17-21, 1993. [PubMed: 8345951]46,XY,der t(1;11)(p22;p13)pat.The balanced translocation was also present in the phenotypically normal father and a brother. The patient had features of Mobius and Poland syndrome, cleft palate, dextrocardia, mandibular hypoplasia, and multiple areas of diffuse brain volume loss.Aberration: Reciprocal translocationMIM#: 173750Index Terms: Mobius syndrome
- Estop A M, Bansal V, Lin A, Levinson F, Karlin S M, Surti U, Wenger S L, Steele M W: Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes. AJMG 49:410-413, 1994. [PubMed: 8160735]Case 3:46,XY,inv(1)(p22p34)de novo.The twins had MCA and died several days after birth.Case from Dr. Surti''s institution.Aberration: Inversion paracentricNegative band
- Francke U, de Martinville B, Coussens L, Ullrich A: The Human gene for the beta subunit of nerve growth factor is located on the proximal short arm of chromosome 1. Science 222:1248-1251, 1983. [PubMed: 6648531]Negative band
- Froster U, Schulte-Korne G, Hebebrand J, Remschmidt H: "Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia." Lancet 342:178-179, 1993. [PubMed: 8101277]46,XY,der(1)der(2)t(1;2)(p22;q31)pat.&"46,XY,t(1;2)(p22;q31)."There was severe delayed speech development and reading and writing disability in this family.Aberration: Reciprocal translocationMIM#: 127700Index Terms: DyslexiaNegative band
- Fryns J P, Kleczkowska A, Kubien E, Petit P, Van den Berghe H: Cytogenetic survey in couples with recurrent fetal wastage. Hum. Genet. 65:336-354, 1984. [PubMed: 6693122]46,XX,t(1;3)(p22;p27).Aberration: Reciprocal translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)Negative band
- Fryns J P, Kleczkowska A, Kubien E, Van den Berghe H: Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patients. Acta Paed. Scand. Suppl. 313:1-23, 1984. [PubMed: 6241420]46,XY,t(1;9)(p22;p24)mat.&46,XX,inv(1)(p22p25)pat.Aberration: ST,IPNegative band
- Fryns J P, Kleczkowska A, Van den Berghe H: Paracentric inversions in man. Hum. Genet. 73:205-213, 1986. [PubMed: 3733076]Family Nos. 2 and 3.46,XX,inv(1)(p22p35)/47,XX,+21,inv(1)(p22p35)pat.&46,XX,inv(1)(p22q36)pat.Aberration: Inversion paracentricNegative band
- Fukushima Y, Kuroki Y, Ito T: "Balanced double complex translocations \46,XX,t(1p;6p;7p;3q;11p)(11q;22p;21q)\ in an infant with multiple congenital anomalies." AJMG 25:313-317, 1986. [PubMed: 3777028]Patient (KCMC-90261) was 1 month old.46,XX,t(1;6;7;11)(11;22;21)(1qter -> p22::11p15 -> 11pter;6qter -> 6p21::1p22 -> 1pter;7qter -> 7p15::6p21 -> 6pter;3pter -> 3q27::7p15 -> 7pter;3qter -> 3q27::11p15 -> 11q11::21q11 -> 21qter;22qter -> 22p11::11q11 -> 11qter;21pter -> 21q11::22p11 -> 22pter).Aberration: Complex translocationNegative band
- Geiger C J, Salzano F M, Mattevi M S, Erdtmann B, da Rocha F J: Chromosome Variation and genetic counseling-20 years of experience in Brazil. Brazil. J. Genet. 10:581-591, 1987.Case 1789; I. M. F. A.. Mother and son were carriers. She had 5 miscarriages. Her parents had normal karyotypes.46,XX or XY,t(1;18)(p22;pter).Aberration: Simple translocationNegative band
- Gordon C T, Krasnewich D, White B, Lenane M, Rapoport J L.: Translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia. J. Autism Develop. Dis. 24:537-545, 1994. [PubMed: 7961336]46,XY,der t(1;7)(p22;q22)pat.,The translocation was familial and present in 3 generations.The patient was 11 years old.Aberration: Reciprocal translocationIndex Terms: Schizophrenia
- Gotter A L, Shaikh T H, Budarf M L, Rhodes C H, Emanuel B S.: A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2. Hum. Mol. Genet. 13:103-115; DOI=10.1093/hmg/ddh004, 2004. [PMC free article: PMC2818528] [PubMed: 14613967]
Rhodes C H, Call K M, Budarf M L, Barnoski B L, Bell C J, Emanuel B S, Bigner S H, Park J P, Mohandas T K.: Molecular studies of an ependymoma-associated constitutional t(1;22)(p22;q11.2). Cytogenet. Cell Genet. 78:247-252, 1997. [PubMed: 9465898]Patient M.L.:46,XY,t(1;22)(p22;q11.2)de novoThe 5 year old was presented with a several-week history of headaches, nausea, and vomitting. The abnormal karyotype was detected prenatally because of advanced maternal age. MRI of the brain revealed a large posterior fossa mass involving the fourth ventricle. Examination of the resection specimen revealed an ependymal neoplasm. Numerous mitoses and areas of tumor necrosis supported the diagnosis of malignant ependymoma.Aberration: Reciprocal translocationIndex Terms: Ependymoma,Palindrome,Low-copy-repeat (LCR-B) - Kalousek D K, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]Observation No. 246,XY,t(1;2)(p22;q31)mat.Observation No. 79.46,XX,t(1;10)(p22;q12)mat.Aberration: Reciprocal translocationNegative band
- McCorquodale M M, Tayel S: "Prenatal detection of de novo 1;5 translocation with the same breakpoints as those identified in a previous unrelated case report." Prenat. Diag. 8:475-476, 1988. [PubMed: 3211850]46,XX,t(1;5)(p22;q26).Normal growth and development.Aberration: Reciprocal translocationNegative band
- Mircher C, Rethore M-O, Lespinasse J, Fert-Ferrer S, Lundsteen C, Kirchoff M.: Interstitial deletion of the short arm of chromosome 1: attempt to establish a clinical phenotype (46,XX,del(1)(p22p32). AJMG DOI=10.1002/ajmg.a.10052; 118A:176-179, 2003. [PubMed: 12655498]46,XX,del(1)(p22p32)de novo.The girl was born in 1995 and has dysmorphic features and developmental delay.Aberration: Interstitial deletionChromosomal Aneuploidy: 1p-
- Miro R, Caballin M R, Pomerol J M, Egozcue J: "A new balanced (1;22)(p22;q13) translocation in a sterile male." Hum. Genet. 71:372, 1985. [PubMed: 4077055]Patient was 42 years old.46,XY,t(1;22)(p22;q13).Aberration: Simple translocationIndex Terms: Sterility ... maleNegative band
- Morichon-Delvallez N, Marchand F: Paracentric inversions in man. Two familial observations. Ann. Genet. 28:119-122, 1985. [PubMed: 3876061]Observation 1: M. et Mme P.46,XY,inv(1)(p22p36).Aberration: Inversion paracentricNegative band
- Neu R L, Miller K, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]Observation No. 150.46,XY,t(1;18)(p22;q21)pat.Observation No. 9046,XX,t(1;11)(p22;p13).Aberration: Reciprocal translocationNegative band
- Palmer C, In, Daniel A, Hook E B, Wulf G: Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. AJMG 33:14-53, 1989. [PubMed: 2750783]Observation No. 9746,XY,t(1;12)(p22;q15)pat.Aberration: Reciprocal translocationNegative band
- Patil S R, Lubs H A, Brown J A, Cohen M M, Gerald P S, Hecht F, Kimberling W J, Myrianthopoulos N, Summitt R L: Incidence of major chromosome abnormalities in children. Cytogenetics 18:302-306, 1977. [PubMed: 880833]Case 4 in this report.46,XX,t(1;2)(p22;q35).&"46,XX,t(1;2)(1qter -> 1p22::2q35 -> 2qter;2pter -> 2q35::1p22 -> 1pter)."&The father and a sib had a balanced Robertsonian translocation t(13q14q).Aberration: Reciprocal translocationNegative band
- Roberts T, Chernova O, Cowell J K.: NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma. Hum. Mol. Genet. 7:1169-1178, 1998. [PubMed: 9618176]t(1;10)(p22;q21)Aberration: Reciprocal translocationIndex Terms: Neuroblastoma,NB4S
- Sachs E S, Jahoda M G J, van Hemel J O, Hoogeboom A J M, Sandkuyl L A: Chromosome studies of 500 couples with two or more abortions. Obst. Gynecol. 65:375-378, 1985. [PubMed: 3974963]46,XY,t(1;8)(p22;p12).Aberration: Reciprocal translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)Negative band
- Siegel S F, Ahdab-Barmada M, Arslanian S, Foley T P, Jr.: Ectopic posterior pituitary tissue and paracentric inversion of the short arm of chromosome 1 in twins. Europ. J. Endocrinol. 133:87-92, 1995. [PubMed: 7627343]46,XY,inv(1)(p22p34)de novoTwins A and B had the same inversion and died at 17 days and 7 weeks of age, respectively.Aberration: Inversion paracentricIndex Terms: Ectopic posterior pituitary tissue
- Smith A, Gaha T J: Data on families of chromosome translocation carriers ascertained because of habitual spontaneous abortion. Aust. N. Z. J. Obst. Gynecol. 30:57-62, 1990. [PubMed: 2346453]Case 7, JF.46,XY,t(1;20)(p22;q12).Aberration: Reciprocal translocationIndex Terms: Spontaneous abortionNegative band
- Teyssier M, Moreau N: Etude chez trois sujets steriles de translocations impliquant le chromosome 1. Bull. Assoc. Anat. 66:263-272, 1982. [PubMed: 7150787]t(1;11)(p22;p11).Aberration: Reciprocal translocationIndex Terms: SterilityNegative band
- van Hemel J O, van Biervliet J P, de Jager van der Grift P W: "A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations." Clin. Genet. 8:213-217, 1975. [PubMed: 1175325]Case A.Y. (210959) in this report.46,XX,t(1;15)(p22;q26).&"46,XX,t(1;15)(1qter -> 1p22::15q26 -> 15qter;15pter -> 15q26::1p22 -> 1pter)."Aberration: Reciprocal translocationNegative band
- Warburton D: De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. AJHG 49:995-1013, 1991. [PMC free article: PMC1683246] [PubMed: 1928105]46,XY,t(1;4)(p22;q23).&"46,XY,t(1;22)(p22;q11.2)."&"46,XX,t(1;16)(p22;p13)."Aberration: Reciprocal translocationNegative band
- Wenger S L, Steele M W, Boone L Y, Lenkey S G, Cummins J H, Chen X Q.: "Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents. AJMG 55: 47-52, 1995. [PubMed: 7702096]It is commented that newborn infants inheriting a seemingly "balanced" karyotype from a normal parent with a balanced reciprocal translocation may still be at an increased risk of being malformed and/or developmentally delayed because of submicroscopic chromosomal imbalances. It is proposed that autosomal fragile sites are unstable areas which predispose to breaks and unequal crossing over near the fragile site breakpoints creating minute duplications and deletions.Case report 2:46,XY,t(1;11)(p22;p13).The child had small mouth, hypertelorism, and apparently low-set ears.Aberration: Reciprocal translocationNegative band
- Yan WL, Guan X-Y, Green E D, Nicolson R, Yap T K, Zhang J, Jacobsen L K, Krasnewich D M, Kumra S, Lenane M C, Gochman P, Damschroder-Williams P J, Esterling L E, Long R T, Martin B M, Sidransky E, Rapoport J L, Ginns E I.: Childhood-Onset Schizophrenia/Autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21. AJMG (Neuropsychiatr. Genet.) 96:749-753, 2000. [PubMed: 11121174]46,XY,der rcp(1;7)(p22;q21.3)pat.,The breakpoint was initially thought to be at 7q22.The patient, at NIMH, had a long history of agitation, autistic behavior. He had dolichostenomelia.Aberration: Reciprocal translocationIndex Terms: Childhood-onset schizophrenia (COS), AutismNo band
- Youings S, Ellis K, Ennis S, Barber J, Jacobs P.: A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities. AJMG DOI=10.1002/ajmg.a.20553; 126A:46-60 , 2003 and 2004. [PubMed: 15039973]Lab ID 8602351:46,XY,t(1;13)(p22;q32)pat.The proband had abnormal phenotype.Lab ID 940631246,XY,t(1;2)(p22;q24)pat.The proband had abnormal phenotype.Lab ID DD9304709:46,XX,t(1;7)(p22;q21.2).The proband had reproductive difficulties.Aberration: Reciprocal translocation