Initial Effect of Recombinant Human Growth Hormone Treatment in a Patient with Lowe Syndrome.

ABSTRACT:

Objectives

Löwe syndrome (the oculocerebrorenal syndrome of Löwe, OCRL, OMIM #309000, ORPHA: 534) is a very rare multisystem X-linked disorder characterized by ocular, kidney and nervous system anomalies.

Case presentation

We present the first Bulgarian genetically confirmed patient with OCRL. The patient had facial dysmorphism, cryptorchidism, congenital cataracts, nystagmus, delayed physical and mental development, and poor nutritional status. He had severe rickets, metabolic acidosis, hypokalaemia, hypophosphataemia, and low IGF-1 levels at the age of three, in addition to his developmental delay. The molecular-genetic analysis reported a pathogenic variant c.1124A>G, p.H375R in the OCRL gene. This variant was inherited from the mother, who was a carrier. Following

SUBMITTER: Iotova V 

PROVIDER: S-EPMC10378625 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature