Luo-Agrawal neurodevelopmental syndrome
MONDO:0981165Mondo
Findings
No curated finding names Luo-Agrawal neurodevelopmental syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Infantile onset · Third trimester onset
HPO, annotations 2026-09-02
Features
85 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal anterior horn cell morphologyHPOHP:0006802
- 1 of 1 reported patient
- Absent speechHPOHP:0001344
- 3 of 3 reported patients
- AnisocoriaHPOHP:0009916
- 1 of 1 reported patient
- Apneic episodes in infancyHPOHP:0005949
- 1 of 1 reported patient
- AspirationHPOHP:0002835
- 1 of 1 reported patient
- Attention deficit hyperactivity disorderHPOHP:0007018
- 1 of 1 reported patient
- ColpocephalyHPOHP:0030048
- 1 of 1 reported patient
- Congenital ptosisHPOHP:0007970
- 1 of 1 reported patient
- Delayed fine motor developmentHPOHP:0010862
- 5 of 5 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- EMG: neuropathic changesHPOHP:0003445
- 1 of 1 reported patient
- Fiber type groupingHPOHP:0033685
- 1 of 1 reported patient
Show the remaining 73
- Gait disturbanceHPOHP:0001288
- 1 of 1 reported patient
- Gastrostomy tube feeding in infancyHPOHP:0011471
- 2 of 2 reported patients
- Generalized hypotoniaHPOHP:0001290
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 5 of 5 reported patients
- Gray matter heterotopiaHPOHP:0002282
- 1 of 1 reported patient
- Happy demeanorHPOHP:0040082
- 1 of 1 reported patient