Psychiatric Phenotype Characterization of Individuals With FOXP1 Syndrome | MicrobiomeTrials← Back to trialsNCT06211673
Psychiatric Phenotype Characterization of Individuals With FOXP1 Syndrome
CompletedOBSERVATIONAL
Trial Details
Start: 2024-01-19Est. Completion: 2025-07-16
Enrollment target: 25 participants Locations- Hôpital Necker-Enfants Malades, Paris, France
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16P11.2 Deletion Syndrome16p11.2 Duplications1Q21.1 Deletion1Q21.1 Microduplication Syndrome (Disorder)ACTL6BADNPAHDC1
ANK2
ANKRD11
ARID1B
ASH1L
BCL11A
CHAMP1
CHD2
CHD8
CSNK2A1
CTBP1
CTNNB1 Gene Mutation
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KATNAL2
KDM5B
KDM6B
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KMT2E
KMT5B
MBD5
MED13L
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PTCHD1
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SETBP1 Gene Mutation
SETD5
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SMARCC2
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SYNGAP1-Related Intellectual Disability
TBR1
ARHGEF9
HNRNPU
PPP3CA
PPP2R1A
SLC6A1
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16P13.11 Microdeletion Syndrome (Disorder)
17Q12 Microdeletion Syndrome (Disorder)
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ACTB
ADSL
AFF2
ALDH5A1
ANK3
ARX
ATRX Gene Mutation
AUTS2 Syndrome
BCKDK
BRSK2
CACNA1C
CAPRIN1
CASK
CASZ1
CHD3
CIC
CNOT3
CREBBP Gene Mutation
CSDE1
CTCF
DEAF1
DHCR7
DLG4
EBF3
EHMT1
EP300 Gene Mutation
GIGYF1
GRIN1
GRIN2D
IQSEC2-Related Syndromic Intellectual Disability
IRF2BPL
KANSL1
KCNB1
KDM3B
NEXMIF
KMT2A
MBOAT7
MEIS2
MYT1L
NAA15
NBEA
NCKAP1
NIPBL
NLGN2
NLGN3
NLGN4X
NR4A2
NRXN1
NRXN2
NSD1 Gene Mutation
PHF21A
PHF3
PHIP
POMGNT1
PSMD12
RELN
RERE
RFX3
RIMS1
RORB
SCN1A
SETD2 Gene Mutation
SHANK2
SIN3A
SLC9A6
SON
SOX5
SPAST
SRCAP
TAOK1
TANC2
TCF20
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WAC
WDFY3
ZBTB20
ZNF292
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9q34 Duplications
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CSNK2B
DYNC1H1
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GNB1
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