Scientists launch major hunt for clues to mysterious metabolic diseases

NCT ID NCT06092346

Recruiting now Knowledge-focused Sponsor: National Human Genome Research Institute (NHGRI) Source: ClinicalTrials.gov ↗

Summary

This study aims to better understand a group of rare genetic disorders that affect how the body processes certain chemicals, which can cause problems with the brain, blood, kidneys, and immune system. Researchers will observe up to 999 participants, including people with these disorders, their family members, and healthy volunteers, collecting samples and health data over time. The goal is to learn what causes these diseases and how they progress, which may help guide future treatments.

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Contacts and locations

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Study contacts

Contact

Phone: •••-•••-•••• Email: •••••@•••••

Locations

National Institutes of Health Clinical Center
RECRUITING

Bethesda, Maryland, 20892, United States

Contact Phone: •••-•••-•••• Email: •••••@•••••

Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.

ADA2, OMIM *607575,SNEDDON SYNDROME; VAIHS ADSL, OMIM *608222, ADENYLOSUCCINATE LYASE DEFICIENCY AICDA, OMIM *605257, IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2 AK1, OMIM *103000, ADENYLATE KINASE DEFICIENCY AMPD1, OMIM *102770, MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY AMPD2, OMIM *102771, SPASTIC PARAPLEGIA 63; PONTOCEREBELLAR HYPOPLASIA AMPD3, OMIM*102772, AMP DEAMINASE DEFICIENCY APRT, OMIM *102600, ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY CAD, *1140120, DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY DHODH, OMIM *126064, MILLER SYNDROME (POSTAXIAL ACROFACIAL DYSOSTOSIS) DPYD, OMIM *274270, DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY DPYS, OMIM *613326, DIHYDROPYRIMIDINASE DEFICIENCY HPRT1, OMIM *308000 LESCH-NYHAN DISEASE IMPDH1, OMIM *146690, RETINITIS PIGMENTOSA TYPE 10, LEBER CONGENITAL AMAURIOSIS TYPE 11 ITPA, OMIM *147520, INOSINE TRIPHOSPHATASE DEFICIENCY; DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 35 METABOLIC DISEASE NT5C3A<TAB>, OMIM *606224, ANEMIA, HEMOLYTIC, DUE TO UMPH1 DEFICIENCY PNP, OMIM *164050, NUCLEOSIDE PHOSPHORYLASE DEFICIENCY PRPS1 DEF, OMIM *311850, ARTS SYNDROME; CHARCOT-MARIE-TOOTH DISEASE PRPS1 SA, OMIM *311850 GOUT, PRPS-RELATED PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY PURINE-PYRIMIDINE METABOLISM SLC22A12, OMIM *607096 HYPOURICEMIA SLC2A9, OMIM *606142 HYPOURICEMIA TPMT, OMIM *187680, THOIPURINES, POOR METABOLISM OF UMPS, OMIM *613891, OROTIC ACIDURIA UNG, OMIM *191525, HYPER-IGM SYNDROME 5 UPB1, OMIM *606673, BETA-UREIDOPROPIONASE DEFICIENCY XDH, OMIM *607633, XANTHINURIA TYPE 1