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48,XYYY syndrome

MONDO:0020469

48,XYYY syndrome is a rare Y chromosome number anomaly that affects only males and is characterized by mild-moderate developmental delay (especially speech), normal to mild intellectual disability, large, irregular teeth with poor enamel, tall stature and acne. Radioulnar stenosis and clinodactyly have also been associated. Boys generally present normal genitalia, while hypogonadism and infertility is frequently reported in adult males.

Also known as: 48,XYYY

6 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Syndromic disease (24) Human disease (14) Aneuploidy (12) Chromosomal disorder (12) Gonosome anomaly (5) Disease of genetic or genomic mechanism (2) Chromosome Y disorder (0) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 1 Not yet finished but already full! 3 Completed 2
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  • New prenatal blood test aims to detect genetic disorders without invasive procedures

    Diagnosis Recruiting now

    This study is testing a new blood test that looks for fetal cells in the mother's blood to detect genetic conditions like Down syndrome. The test will be compared to standard diagnostic methods such as amniocentesis or newborn testing. The study involves 1,000 pregnant individual…

    Sponsor: BillionToOne Inc. • Aim: Diagnosis

    Last updated Jun 27, 2026 13:06 UTC

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