Paternal 20q13.2q13.3 microdeletion syndrome
MONDO:0016842Paternal 20q13.2q13.3 microdeletion syndrome is a recently described syndrome characterized by severe pre- and post-natal growth retardation, microcephaly, intractable feeding difficulties, mild psychomotor retardation, hypotonia and facial dysmorphism.
Also known as: paternal 20q13.2-q13.3 microdeletion syndrome, paternal del(20)(q13.2q13.3), paternal monosomy 20q13.2-q13.3, paternal monosomy 20q13.2q13.3
2 clinical trials for this condition and its sub-types.
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Disease
(618)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 20 disorder
(0)
Disease by etiologic mechanism
(0)
Partial deletion of chromosome 20
(0)
Partial deletion of the long arm of chromosome 20
(0)
Syndrome caused by partial chromosomal deletion
(0)