Combination of thrombocytopenia and hypocalcemia may indicate the possibility of Stormorken Syndrome with STIM1 mutation
Saved in:
| Main Authors: | Chen-Hua Wang, Wen-Chen Liang, Pei-Chin Lin, Yuh-Jyh Jong |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2022-03-01
|
| Series: | Pediatrics and Neonatology |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1875957221001790 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Clinical variability in STIM1 variant c.262A>G associated with Stormorken syndrome
by: L. Silva-Hernández, et al.
Published: (2025-01-01) -
Life-threatening Dilated Cardiomyopathy Induced by Late-onset Neonatal Hypocalcemia
by: Po-Ching Chou, et al.
Published: (2016-12-01) -
Evolutionary history of calcium-sensing receptors unveils hyper/hypocalcemia-causing mutations.
by: Aylin Bircan, et al.
Published: (2024-11-01) -
Limb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan
by: Chien-Hua Wang, et al.
Published: (2015-02-01) -
Bilateral Papilledema in Hypocalcemia
by: JL Goyal, et al.
Published: (2012-10-01)