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49, XXXXY

49, XXXXY syndrome
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-2 of 2 results.
GROWing Up With Rare GENEtic Syndromes
Status: Recruiting
Last Changed: Jul 09, 2020
First Received: Jul 09, 2020
Disease(s): Prader-Willi Syndrome, PWS-like Syndrome, Silver Russel Syndrome, Congenital Hypopituitarism, Klinefelter (XXY-)Syndrome, Congenital Adrenal Hyperplasia, XXXXY Syndrome, XXYY Syndrome, XXXX Syndrome (Tetra-X Syndrome), Disorders of Sex Development, Turner Syndrome, 46, XY DSD, Tuberous Sclerosis, Neurofibromatosis, Albright Hereditaire Osteodystrofie, Cornelia de Lange Syndrome, Saethre-Chotzen Syndrome, 17p- Deletiesyndrome, VCF Syndrome, POLR3A Mutatie, Ohdo Syndrome, Jacobsen Syndrome / 11 q Syndrome, Myrhe Syndrome, CHARGE Syndrome, 1q25-32 Deletie, Bardet Biedl Syndrome, Rett Syndrome, 22q11 Deletion Syndrome, Allan-Herndon-Dudley Syndrome, Kallmann Syndrome, Rare Bone Disorders, Noonan Syndrome, Williams-Beuren Syndrome
Intervention(s): Retrospective file studies
Locations: Erasmus Medical Center, Rotterdam, Zuid-Holland, Netherlands
The eXtroardinarY Babies Study: Natural History of Health and Neurodevelopment in Infants and Young Children With Sex Chromosome Trisomy
Status: Recruiting
Last Changed: Jan 22, 2020
First Received: Jan 11, 2018
Disease(s): Klinefelter Syndrome, Trisomy X, XYY Syndrome, XXXY and XXXXY Syndrome, Xxyy Syndrome, Xyyy Syndrome, Xxxx Syndrome, Xxxxx Syndrome, Xxxyy Syndrome, Xxyyy Syndrome, Xyyyy Syndrome, Male With Sex Chromosome Mosaicism
Intervention(s): Assessments of Development and Growth
Locations: Children's Hospital Colorado, Aurora, Colorado, United States
Nemours at Thomas Jefferson University, Philadelphia, Pennsylvania, United States