FOXG1 syndrome due to 14q12 microdeletion

Orpha code: 261144OMIM code:

Definition

14q12 microdeletion syndrome is a recently described syndrome characterized by severe intellectual deficit, with a normal neonatal period, followed by a phase of regression at the age of 3-6 months.

Disease data
Classification

Clinical subtype

Synonyms
Del(14)(q12)
Del(14)(q12)
Monosomia 14q12
Monosomy 14q12
ORPHA code
261144
OMIM code
-
ICD10 code
Q93.5
ICD11 code
-

No additional description.

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