All individuals with variants in gene TXNRD2

7 entries on 1 page. Showing entries 1 - 7.
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00050212 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050438 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected father/child F - United Kingdom (Great Britain) - - - Decipher - ? sparse scalp hair, fragile nails, abnormality of limb bone morphology, alopecia of scalp, high palate, global developmental delay, global developmental delay, abnormality of the heart 1 2 Johan den Dunnen
00050514 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? agenesis of corpus callosum, periventricular gray matter heterotopia, seizures, frontal bossing, eczema 1 1 Johan den Dunnen
00050542 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? abnormality of the nervous system, dysphagia, abnormality of the palpebral fissures, inverted nipples, redundant skin, global developmental delay 1 1 Johan den Dunnen
00050613 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? specific learning disability, congenital hypothyroidism, abnormality of metabolism/homeostasis, rhabdomyolysis, cardiomyopathy 1 1 Johan den Dunnen
00301734 17-3959 PubMed: Maddirevula 2019 - M - Saudi Arabia - - - - - ? history of recurrent hypoglycemia, polycythemia. He has history of congenital heart disease (truncus arteriosus, and pulmonary stenosis). Examination revealed dysmorphic facies (hypertelorism, synophrys, bitemporal narrowing, bulbous nose, thick lips, short neck, cleft palate, large omphalocele, and clubbing of fingers). He was also diagnosed with glucocorticoid deficiency. 1 1 Johan den Dunnen
00320299 BPP1 PubMed: Isbister 2020 - - - Australia - - - - - CM survived sudden cardiac arrest 1 1 Johan den Dunnen
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