Hartsfield syndrome

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Name:
Hartsfield syndrome
Description:
A rare, genetic, multiple congenital anomalies syndrome characterized by variable expression of the holoprosencephaly (HPE) spectrum in association with ectrodactyly, cleft lip/palate and/or other ectodermal anomalies. Developmental delay of variable severity and endocrine abnormalities are often associated.
ORPHAcode:
2117
Synonyms:
Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14