Disease #03471 (RP59;CDG1BB (retinitis pigmentosa, type 59 (RP59, glycosylation, congenital disorder of, type Ibb (CDG1BB))), OMIM:613861)

Official abbreviation RP59;CDG1BB
Name retinitis pigmentosa, type 59 (RP59, glycosylation, congenital disorder of, type Ibb (CDG1BB))
OMIM ID 613861
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene DHDDS
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00409271 ? PubMed: Sabry 2016 - M no - - 00y08m - - - RP59;CDG1BB intra-uterine growth retardation and decreased fetal movements; born at 37 weeks of gestation with a weight of 2090 g (-3.25 SD), a length of 42 cm (-4 SD), an occipitofrontal circumference of 32 cm (-2 SD) and Apgar score 10/10; two episodes of severe bradycardia during the first day of life and was transferred to an intensive care unit; axial hypotonia, peripheral hypertonia, enlarged liver, micropenis and cryptorchidism; transient increase of serum transaminases, renal failure; developed epilepsy; liver sonography: mild dilatation of the biliary duct; little psychomotor acquisitions, no eye contact, poor sucking with frequent regurgitations; failure to thrive; 2 months: fundus: pale papillae, electroretinogram: showed no response to any type of stimulation; brainstem evoked auditory potentials: sensorineural deafness with an auditory threshold of 90 dB (right ear) and 100 dB (left ear); died at 8 months during a status epilepticus DHDDS ALG6, DHDDS 3 1 LOVD
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