||
8q22.1 microdeletion syndrome (disorder)
8q22.1 microdeletion syndrome
Nablus mask-like facial syndrome
Monosomy 8q22.1
A rare microdeletion syndrome associated with a distinct facial appearance. It has been reported in four unrelated patients. A mask-like facial appearance is the most characteristic feature with blepharophimosis, tight appearing glistening facial skin, flat and broad nose, dysplastic ears and unusual scalp hair pattern. Camptodactyly, joint contractures, unusual dentition and mild developmental delay can be observed. Cryptorchidism in boys and a happy disposition are constant.
8q22.1-microdeletiesyndroom
syndroom van 8q22.1-microdeletie
'Nablus mask-like facial'-syndroom
monosomie 8q22.1
Id719664004
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteFace structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyPartial monosomy
Finding siteChromosome pair 8
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDeletion of long arm
Finding siteChromosome pair 8
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ93.5
RuleTRUE
AdviceALWAYS Q93.5
CorrelationSNOMED CT source code to target map code correlation not specified