scholarly journals Ring chromosome 15 syndrome presenting with gonadotropin dependent precocious puberty

2021 ◽  
Vol 50 (4) ◽  
pp. 718
Author(s):  
B. C. Lakmini ◽  
J. Suntharesan ◽  
U. A. M. D. De Silva ◽  
Navoda Atapattu
Keyword(s):  
Precocious Puberty ◽  
Ring Chromosome ◽  
Chromosome 15

Ring chromosome 12 resulting from nonrandom telomeric associations with the short arm of chromosome 15 in a cerebellar astrocytoma

1993 ◽  
Vol 8 (2) ◽  
pp. 69-73 ◽  
Author(s):  
Jeffrey R. Sawyer ◽  
Gael Sammartino ◽  
M. Husain ◽  
Jane M. Lewis ◽  
Bruce Anderson ◽  
...  
Keyword(s):  
Ring Chromosome ◽  
Chromosome 12 ◽  
Chromosome 15 ◽  
Cerebellar Astrocytoma

Molecular cytogenetic characterization of ring chromosome 15 in three unrelated patients

2004 ◽  
Vol 130A (4) ◽  
pp. 340-344 ◽  
Author(s):  
Z. Tümer ◽  
T.L. Harboe ◽  
E. Blennow ◽  
V.M. Kalscheuer ◽  
N. Tommerup ◽  
...  
Keyword(s):  
Ring Chromosome ◽  
Chromosome 15 ◽  
Molecular Cytogenetic ◽  
Cytogenetic Characterization

Ring chromosome 15 in a male adult with radial defects. Evaluation of the phenotype

2008 ◽  
Vol 18 (6) ◽  
pp. 428-433 ◽  
Author(s):  
Peter Meinecke ◽  
Thea Koske-Westphal
Keyword(s):  
Ring Chromosome ◽  
Chromosome 15 ◽  
Male Adult

Ring chromosome 15: characterization by array CGH

2005 ◽  
Vol 118 (5) ◽  
pp. 611-617 ◽  
Author(s):  
Ian A. Glass ◽  
Katherine A. Rauen ◽  
Emily Chen ◽  
Jillian Parkes ◽  
Donna G. Alberston ◽  
...  
Keyword(s):  
Array Cgh ◽  
Ring Chromosome ◽  
Chromosome 15

scholarly journals Two patients with ring chromosome 15 syndrome

1988 ◽  
Vol 29 (1) ◽  
pp. 149-154 ◽  
Author(s):  
Merlin G. Butler ◽  
Agnes B. Fogo ◽  
David A. Fuchs ◽  
Francis S. Collins ◽  
Viathilingam G. Dev ◽  
...  
Keyword(s):  
Ring Chromosome ◽  
Chromosome 15

Ring chromosome 15:r(15). Identification by R banding

1975 ◽  
Vol 27 (3) ◽  
pp. 259-262 ◽  
Author(s):  
C. Stoll ◽  
J. G. Juif ◽  
J. C. Luckel ◽  
C. Lausecker
Keyword(s):  
Ring Chromosome ◽  
Chromosome 15

De Novo Ring Chromosome 15: Molecular Cytogenetic and Clinical Characterization of First Case from Saudi Arabia

2020 ◽  
Author(s):  
Amal Alhashem ◽  
Saria Alazmeh ◽  
Ayla Barakat ◽  
Ahmed Alfares ◽  
Hatem Elghezal
Keyword(s):  
De Novo ◽  
Ring Chromosome ◽  
Chromosome 15 ◽  
Chromosomal Disorder ◽  
First Case ◽  
Café Au Lait Spots ◽  
New Findings ◽  
Crossed Fused Renal Ectopia ◽  
Variable Presentation

AbstractRing chromosome 15 is a rare chromosomal disorder, which usually occurs during early embryonic development via spontaneous errors and has variable presentation. To date, 89 cases of this condition have been reported. This case report describes a 5-year-old Saudi boy who was diagnosed as having de novo 46,XY,r(15). The patient presented with short stature, speech delay, café au lait spots, and facial dysmorphic features, together with new findings of left crossed fused renal ectopia and 11 ribs. This presentation was compared with the findings of cases reported previously.

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