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Hydrolethalus syndrome

MONDO:0006037

Hydrolethalus (HLS) is a severe fetal malformation syndrome characterized by craniofacial dysmorphic features, central nervous system, cardiac, respiratory tract and limb abnormalities.

Also known as: HLS, hydrolethalus

1 clinical trial for this condition and its sub-types.

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Sub-types

Hydrolethalus syndrome 1 (1) Hydrolethalus syndrome 2 (0)

Broader categories

Disease (679) Hereditary disease (176) Human disease (14) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0) Disease by etiologic mechanism (0)
Trials to join now! 1
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  • Scientists map DNA 'Signatures' in rare fetal diseases

    Knowledge-focused Recruiting now

    This study looks at DNA methylation patterns (chemical tags on DNA) in fetuses with rare genetic diseases. Researchers will analyze DNA from amniotic fluid and tissue samples to create reference signatures. The goal is to improve diagnosis of these conditions before birth. The st…

    Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:01 UTC

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