نتایج جستجو برای: monosomy 21

تعداد نتایج: 249214  

Journal: :Journal of medical genetics 2000
P Lichtner R König T Hasegawa H Van Esch T Meitinger S Schuffenhauer

Partial monosomy 10p is a rare chromosomal condition and a significant proportion of patients show features of DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). A critical haploinsufficiency region for DGS/VCFS was defined on 10p (DGCR2). We performed molecular deletion analysis of two further patients with partial monosomy 10p, who showed hypoparathyroidism, deafness, and renal dys...

2015
A J Greenberg S Philip A Paner S Velinova A Badros R Catchatourian R Ketterling R A Kyle S Kumar C M Vachon S V Rajkumar

We examined four clinically assessed cytogenetic subtypes (t(11;14), t(4;14), monosomy 13/del13q and monosomy 17/del17p in 292 black patients with newly diagnosed multiple myeloma (MM) from four medical centers, who had fluorescent in situ hybridization testing results available in their medical records. We then compared the prevalence of these abnormalities with a previously characterized Mayo...

2016
Kohei Kasahara Masahiro Onozawa Naohiro Miyashita Emi Yokohata Miho Yoshida Minoru Kanaya Mizuha Kosugi-Kanaya Ryo Takemura Shojiro Takahashi Junichi Sugita Akio Shigematsu Mutsumi Takahata Shinichi Fujisawa Daigo Hashimoto Katsuya Fujimoto Tomoyuki Endo Takeshi Kondo Takanori Teshima

We report a case of acute myeloid leukemia (AML) with two cytogenetically unrelated clones. The patient was a 45-year-old male who was diagnosed with acute monoblastic leukemia (AMoL). Initial G-band analysis showed 51,XY,+6,+8,inv(9)(p12q13)c,+11,+13,+19[12]/52,idem,+Y[8], but G-band analysis after induction therapy showed 45,XY,-7,inv(9)(p12q13)c[19]/46,XY,inv(9)(p12q13)c[1]. Retrospective FI...

Journal: :American journal of medical genetics. Part A 2013
Shane C Quinonez John M Park Raja Rabah Kailey M Owens Beverly M Yashar Thomas W Glover Catherine E Keegan

Deletion of the distal segment of 9p causes a syndrome comprising trigonocephaly, minor anomalies, and intellectual disability. Patients with this condition also frequently present with genitourinary abnormalities including cryptorchidism, hypospadias, ambiguous genitalia, or 46,XY testicular dysgenesis. The region responsible for the gonadal dysgenesis has been localized to 9p24.3 with the lik...

2016
Pınar Zengin Akkuş Arda Çetinkaya Deniz Çağdaş Ayvaz Mehmet Alikaşifoğlu Ayfer Alikaşifoğlu İlhan Tezcan Koray Boduroğlu

Monosomy 18p is a relatively frequent deletion syndrome with an estimated frequency of one in 50,000 liveborns. Most frequent findings consist of mild to moderate growth deficiency, intellectual disability, microcephaly, and facial dysmorphic features including ptosis, epicanthic folds, low nasal bridge, hypertelorism and large protruding ears. Anomalies of other systems may accompany. A 31-yea...

Journal: :Journal of medical genetics 1990
D R Romain J Goldsmith H Cairney L M Columbano-Green R H Smythe R G Parfitt

An 18 month old girl with partial monosomy for the long arm of chromosome 22 is described. The karyotype was 46,XX,del(22)(pter----q13.1::q13.33----qter). To our knowledge this is the first report of monosomy for this specific segment of chromosome 22. Clinical features include developmental delay in all areas, hypotonia, macrosomia, full cheeks, eyebrows, and eyelids, mild epicanthus, wide nas...

Journal: :Fetal diagnosis and therapy 2014
Argyro Syngelaki Eugene Pergament Tessa Homfray Ranjit Akolekar Kypros H Nicolaides

OBJECTIVE To estimate the proportion of other chromosomal abnormalities that could be missed if combined testing was replaced by cell-free (cf) DNA testing as the method of screening for trisomies 21, 18 and 13. METHODS The prevalence of trisomies 21, 18 or 13, sex chromosome aneuploidies, triploidy and other chromosomal abnormalities was examined in pregnancies undergoing first-trimester com...

Journal: :Chromosome Research 2009

Journal: :Archives of Disease in Childhood 1969

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