All individuals with variants in gene XPR1

7 entries on 1 page. Showing entries 1 - 7.
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00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00184631 - - 2-generation family, 2 affecteds (2F) F no China - - - - - IBGC6 brain calcifications 1 2 Wanjin Chen
00184632 - - 2-generation family, 7 affecteds (2F, 5M) F ? China - - - - - IBGC6 brain calcifications, orofacial dyskinesia, mild anxiety 1 7 Wanjin Chen
00426198 10DK15900 PubMed: Al-Kasbi 2022 patient, other affecteds in family F yes Oman - - - - - ID Variable signs of cardiomyopathy, neonatal pulmonary hypertension, hypophosphatemia, chronic lung disease, developmental delay, and brain basal ganglia calcification 1 1 Johan den Dunnen
00426199 10MS4500 PubMed: Al-Kasbi 2022 patient, other affecteds in family F yes Oman - - - - - ID Variable signs of cardiomyopathy, neonatal pulmonary hypertension, hypophosphatemia, chronic lung disease, developmental delay, and brain basal ganglia calcification 1 1 Johan den Dunnen
00426200 50DK4600 PubMed: Al-Kasbi 2022 patient, other affecteds in family M yes Oman - - - - - ID Variable signs of cardiomyopathy, neonatal pulmonary hypertension, hypophosphatemia, chronic lung disease, developmental delay, and brain basal ganglia calcification 1 1 Johan den Dunnen
00426201 63MS1200 PubMed: Al-Kasbi 2022 patient, other affecteds in family M yes Oman - - - - - ID Variable signs of cardiomyopathy, neonatal pulmonary hypertension, hypophosphatemia, chronic lung disease, developmental delay, and brain basal ganglia calcification 1 1 Johan den Dunnen
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