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Holoprosencephaly

Holoprosencephaly (HPE) is a complex brain malformation resulting from incomplete cleavage of the prosencephalon, occurring between the 18th and 28th day of gestation, and affecting both the forebrain and face, which results in neurological manifestations and facial anomalies of variable severity.

0 trials tagged with this condition →

Alobar holoprosencephaly 0 trials Sub-types →
Chromosome 1q41-q42 deletion syndrome 0 trials
Holoprosencephaly 1 0 trials
Holoprosencephaly 10 0 trials
Holoprosencephaly 11 0 trials
Holoprosencephaly 12 with or without pancreatic agenesis 0 trials
Holoprosencephaly 13, X-linked 0 trials
Holoprosencephaly 14 0 trials
Holoprosencephaly 2 0 trials
Holoprosencephaly 3 0 trials Sub-types →
Holoprosencephaly 4 0 trials
Holoprosencephaly 6 0 trials
Holoprosencephaly 7 0 trials
Holoprosencephaly 8 0 trials
Lobar holoprosencephaly 0 trials Sub-types →
Microform holoprosencephaly 0 trials Sub-types →
Semilobar holoprosencephaly 0 trials