Cerebral Palsy, Spastic Quadriplegic, 3; Cpsq3
Genes related to Cerebral Palsy, Spastic Quadriplegic, 3; Cpsq3
Clinical FeaturesTop most frequent phenotypes and symptoms related to Cerebral Palsy, Spastic Quadriplegic, 3; Cpsq3
- Global developmental delay
- Cognitive impairment
- Abnormal pyramidal sign
And another 9 symptoms. If you need more information about this disease we can help you.
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Cerebral Palsy, Spastic Quadriplegic, 3; Cpsq3 Recommended genes panels
|Panel Name, Specifity and genes Tested/covered|
Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel.
By CeGaT GmbH (Germany).
RTN2, SACS, AIMP1, SLC16A2, SLC1A4, SLC25A15, SOD1, SOX10, SPG11, ATL1, SPAST, SPG7, SPR, STUB1, TARDBP, TFG, TH, UBQLN2, VAMP1, VAPB , (...)
View the complete list with 122 more genes
By Fulgent Genetics Fulgent Genetics (United States).
You can get up to -6 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.OMIM Rare Disease Search Engine
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4 BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD NANCE-HORAN SYNDROME; NHS CAREY-FINEMAN-ZITER SYNDROME; CFZS MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49 BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES