Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Distal Hereditary Motor Neuropathies: A Rare Familial Case Caused by a Mutation in the VWA1 Gene

View through CrossRef
Distal hereditary motor neuropathies (dHMN) include 7 categories according to the mode of transmission, age of onset, topography of the deficit, and presence of associated signs. Recently, the VWA1 gene has been identified as responsible for dHMN with autosomal recessive inheritance, manifesting by muscle weakness starting in childhood or adulthood. We report the case of a 50-year-old patient presenting with dHMN with a mutation of the VWA1 gene. The patient, the first born of non-consanguineous parents, presented with a lower limb deficit initially diagnosed as spinal muscular atrophy (SMA). His sister has also motor neuropathy since childhood. Symptoms began early, with delayed acquisition of sitting and walking. Clinical examination revealed a disto-proximal deficit in all four limbs, predominating in the lower limbs, a discrete static cerebellar syndrome, and asymmetric dysmetria. Diffuse amyotrophy of the legs persisted, particularly in the tibialis anterior. Electroneuromyogram confirmed distal motor neuropathy, and muscles MRI showed symmetrical fatty degeneration of the muscles, marked in the pelvis and distal lower limbs. The genetic panel excluded proximal SMA and the classic mutations of peripheral neuropathies. A homozygous variation in the VWA1 gene (NM_022834.5:c.62_71dup) was identified, confirming the diagnosis of dHMN linked to this gene. Conclusion: This case illustrates the genetic variability of dHMN and the importance of extending genetic analyses to include emerging mutations such as those in the VWA1 gene. Keywords: neuropathies, hereditary, gene.
Title: Distal Hereditary Motor Neuropathies: A Rare Familial Case Caused by a Mutation in the VWA1 Gene
Description:
Distal hereditary motor neuropathies (dHMN) include 7 categories according to the mode of transmission, age of onset, topography of the deficit, and presence of associated signs.
Recently, the VWA1 gene has been identified as responsible for dHMN with autosomal recessive inheritance, manifesting by muscle weakness starting in childhood or adulthood.
We report the case of a 50-year-old patient presenting with dHMN with a mutation of the VWA1 gene.
The patient, the first born of non-consanguineous parents, presented with a lower limb deficit initially diagnosed as spinal muscular atrophy (SMA).
His sister has also motor neuropathy since childhood.
Symptoms began early, with delayed acquisition of sitting and walking.
Clinical examination revealed a disto-proximal deficit in all four limbs, predominating in the lower limbs, a discrete static cerebellar syndrome, and asymmetric dysmetria.
Diffuse amyotrophy of the legs persisted, particularly in the tibialis anterior.
Electroneuromyogram confirmed distal motor neuropathy, and muscles MRI showed symmetrical fatty degeneration of the muscles, marked in the pelvis and distal lower limbs.
The genetic panel excluded proximal SMA and the classic mutations of peripheral neuropathies.
A homozygous variation in the VWA1 gene (NM_022834.
5:c.
62_71dup) was identified, confirming the diagnosis of dHMN linked to this gene.
Conclusion: This case illustrates the genetic variability of dHMN and the importance of extending genetic analyses to include emerging mutations such as those in the VWA1 gene.
Keywords: neuropathies, hereditary, gene.

Related Results

Hydatid Disease of The Brain Parenchyma: A Systematic Review
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Abstarct Introduction Isolated brain hydatid disease (BHD) is an extremely rare form of echinococcosis. A prompt and timely diagnosis is a crucial step in disease management. This ...
Analysis of SMOC2 gene variants in familial and non-familial primary open angle glaucoma Pakistani patients
Analysis of SMOC2 gene variants in familial and non-familial primary open angle glaucoma Pakistani patients
AIM: To find out the association of secreted protein acidic and rich in cysteine (SPARC)-related modular calcium binding 2 (SMOC2) gene variants rs2255680 and rs13208776 with genot...
Hereditary Neuropathies: Update 2017
Hereditary Neuropathies: Update 2017
AbstractHereditary neuropathy is an umbrella term for a group of nonsyndromic conditions with a prevalence of approximately 1:2,500. In addition to the most frequent form, Charcot–...
Age-stratified mosaic of neuropathies: a comprehensive analysis of the prevalence and patterns in different age groups
Age-stratified mosaic of neuropathies: a comprehensive analysis of the prevalence and patterns in different age groups
Background and Objective: Neuropathies pose significant challenges in diagnosis and management due to their heterogeneous etiologies, varied clinical presentations, and differenti...
Familial hypercholesterolaemia
Familial hypercholesterolaemia
Abstract Familial hypercholesterolaemia (OMIM 143890) is characterized by hypercholesterolaemia from birth, with the subsequent development of cutaneous and tendon x...
Distal Hereditary Motor Neuropathy With SIGMAR 1 Mutation: 2 Cases at Fann University Hospital, Dakar, Senegal
Distal Hereditary Motor Neuropathy With SIGMAR 1 Mutation: 2 Cases at Fann University Hospital, Dakar, Senegal
Introduction: Distal hereditary motor neuropathies (dHMN) constitute a rare heterogeneous group of disorders characterized by degeneration of the motor component of peripheral nerv...
Expression and polymorphism of genes in gallstones
Expression and polymorphism of genes in gallstones
ABSTRACT Through the method of clinical case control study, to explore the expression and genetic polymorphism of KLF14 gene (rs4731702 and rs972283) and SR-B1 gene...

Back to Top