Introduction Pallister-Hall syndrome (PHS) is a rare autosomal dominant disorder caused by pathogenic variants in GLI3 gene. It is characterized by variable combinations of hypothalamic hamartoma, polydactyly, bifid epiglottis, renal and genitourinary abnormalities, imperforate anus, and pituitary dysfunction. Most cas...
Noha N. Mukhtar, Montaha W. Demyati, Allianah D. Benito et al.· Frontiers in Endocrinology· 0 citations
A patient with longstanding myotonia congenita due to a CLCN1 variant in whom an incidental discovery of severe hypocalcemia led to the diagnosis of GNAS-related pseudohypoparathyroidism (PHP), demonstrating two clinically expressed Mendelian disorders together with a third actionable molecular finding.
Noha N. Mukhtar, Deema Alturki, Allianah D. Benito et al.· Frontiers in Endocrinology· 0 citations
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