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Browse result for Delpire-McNeill syndrome

※ introduction

    Delpire-McNeill syndrome (DELMNES) is a neurodevelopmental disorder with highly variable manifestations. Patients present in infancy with global developmental delay, including motor, speech, and impaired intellectual development. The most severely affected patients have hypotonia, inability to hold their head or walk, bilateral sensorineural deafness, and absent language, whereas others have delayed walking and mild to moderate intellectual disability, often with speech delay and autistic features. More variable features may include spasticity or minor involvement of other organ systems, such as hip dislocation or ventricular septal defect.

Reference
OMIM: Delpire-McNeill syndrome



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD05605P550116558
SLC12A2
Solute carrier family 12 member 2 -chloride cotransporter 2)
Homo sapiens