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1.

Jeffries-Lakhani neurodevelopmental syndrome

Jeffries-Lakhani neurodevelopmental syndrome (JELANS) is an autosomal recessive disorder characterized by hypotonia, early-onset seizures, and global developmental delay apparent from infancy. Affected individuals have motor delay, speech delay, and impaired intellectual development, and about half of patients are nonambulatory and/or nonverbal. Some patients have cardiac arrhythmia, but congenital cardiac septal defects are only rarely observed. Additional features may include feeding difficulties, recurrent infections, ocular defects, and nonspecific dysmorphic features. Premature death due to cardiac arrhythmia or epilepsy may occur (Jeffries et al., 2024). [from OMIM]

MedGen UID:
1854360
Concept ID:
C5935596
Disease or Syndrome
2.

Oral aversion

Reluctance or refusal of a child to be breastfed or eat, manifested as gagging, vomiting, turning head away from food, or avoidance of sensation in or around the mouth (i.e. toothbrushing or face-washing). [from HPO]

MedGen UID:
786047
Concept ID:
C3665983
Mental or Behavioral Dysfunction
3.

Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies

MedGen UID:
318752
Concept ID:
C1832950
Disease or Syndrome
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