Neonatal hypoparathyroidism can be part of the DiGeorge syndrome (dysmorphic facies, cardiac defects, immune deficiency, and hypoparathyroidism) due to a microdeletion (or other genetic abnormalities) on chromosome 22q11.2.
The HDR syndrome (hypoparathyroidism, sensorineural deafness, and renal anomalies) due to mutations in or deletion of an allele of the GATA3 transcription factor; and other rare conditions.
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