» Articles » PMID: 1536799

The Neurologic Aspects of Transcobalamin II Deficiency

Overview
Journal Br J Haematol
Specialty Hematology
Date 1992 Jan 1
PMID 1536799
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Thirty-four symptomatic cases of inherited transcobalamin II (TCII) deficiency were analysed in order to determine the frequency and nature of neurologic manifestations. In no instance was there definite evidence of a neurologic disorder at the time of presentation as a young infant. One child of 2 1/2 years transiently lost deep tendon reflexes at a time of suboptimal treatment. A syndrome of mental retardation and other neurologic manifestations was observed in three cases, all with the following in common: (1) an extended duration of illness of 2-17 years; (2) inadequate or not treatment with Cbl; (3) treatment with folic of folinic acid. TCII deficiency rarely if ever presents with neurologic manifestations. However, neurologic disorders can be produced subsequently by improper treatment.

Citing Articles

Determination of plasma transcobalamin-II and zinc levels in newly-diagnosed and long-standing grand mal epileptic patients.

Aman-Mohammady A, Saadat P, Qujeq D, Hajian-Tilaki K, Saleki K Caspian J Intern Med. 2023; 14(2):199-204.

PMID: 37223292 PMC: 10201111. DOI: 10.22088/cjim.14.2.199.


A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency.

Pongphitcha P, Sirachainan N, Khongkraparn A, Tim-Aroon T, Songdej D, Wattanasirichaigoon D BMC Pediatr. 2022; 22(1):233.

PMID: 35488219 PMC: 9052601. DOI: 10.1186/s12887-022-03291-5.


Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene: a case report.

Martino F, Magenta A, Troccoli M, Martino E, Torromeo C, Putotto C Ital J Pediatr. 2021; 47(1):54.

PMID: 33685478 PMC: 7941906. DOI: 10.1186/s13052-021-01007-6.


Transcobalamin deficiency: vitamin B deficiency with normal serum B levels.

Khera S, Pramanik S, Patnaik S BMJ Case Rep. 2019; 12(10).

PMID: 31666257 PMC: 6827761. DOI: 10.1136/bcr-2019-232319.


Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Unal S, Rupar T, Yetgin S, Yarali N, Dursun A, Gursel T Turk J Haematol. 2015; 32(4):317-22.

PMID: 25914105 PMC: 4805327. DOI: 10.4274/tjh.2014.0154.