Introduction: Hereditary sensory and autonomic neuropathies type V (HSAN type V) is the rarest of sensory neuropathies. The main features are loss of deep sensitivity as well as self-mutilation of especially the lips, fingers, tongue and teeth. Case Report: In this article we report a rare case of a 4-year-old child with HSAN type V. the patient’s management had two aims first reinforce parental and child compliance and then restore function and aesthetic. Discussion: The diagnosis of a HSAN type V relies not only on the clinical features but also on the genetic analysis. Dental management and careful monitoring are key elements in maintaining social, psychological and behavioral equilibrium of these patients
How to Cite This Article: Azadvari M, Emami Razavi SZ, Kazemi Sh. Hereditary Sensory and Autonomic N...
Hereditary Sensory and Autonomic Neuropathy (HSAN) is a rare group of diseases involving varying deg...
Hereditary Sensory Autonomic Neuropathy II (HSAN II) is a rare genetic disorder, characterized by se...
Hereditary sensory and autonomic neuropathy (HSAN) is a rare syndrome which is seen in early childho...
Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic syndromes of unknown etiology....
Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic syndromes of unknown etiolog...
Several types of hereditary sensory and autonomic neuropathies (HSAN) are reported in literatures. W...
Background and purpose: Hereditary sensory and autonomic neuropathy ( HSAN) type V is a very rare di...
Hereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by inse...
severe hereditary sensory neuropathy The hereditary sensory and autonomic neuropathies (HSAN) are ra...
Abstract Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic disorders that often ...
SummaryHereditary sensory and autonomic neuropathy type IV (HSAN-IV) is a very rare autosomal recess...
severe hereditary sensory neuropathy The hereditary sensory and autonomic neuropathies (HSAN) are ra...
Hereditary sensory autonomic neuropathies (HSAN) are rare forms of chronic neuropathies in children,...
Hereditary sensory and autonomic neuropathy type V (HSAN V) is an autosomal recessive disorder chara...
How to Cite This Article: Azadvari M, Emami Razavi SZ, Kazemi Sh. Hereditary Sensory and Autonomic N...
Hereditary Sensory and Autonomic Neuropathy (HSAN) is a rare group of diseases involving varying deg...
Hereditary Sensory Autonomic Neuropathy II (HSAN II) is a rare genetic disorder, characterized by se...
Hereditary sensory and autonomic neuropathy (HSAN) is a rare syndrome which is seen in early childho...
Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic syndromes of unknown etiology....
Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic syndromes of unknown etiolog...
Several types of hereditary sensory and autonomic neuropathies (HSAN) are reported in literatures. W...
Background and purpose: Hereditary sensory and autonomic neuropathy ( HSAN) type V is a very rare di...
Hereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by inse...
severe hereditary sensory neuropathy The hereditary sensory and autonomic neuropathies (HSAN) are ra...
Abstract Hereditary sensory and autonomic neuropathies (HSAN) are rare genetic disorders that often ...
SummaryHereditary sensory and autonomic neuropathy type IV (HSAN-IV) is a very rare autosomal recess...
severe hereditary sensory neuropathy The hereditary sensory and autonomic neuropathies (HSAN) are ra...
Hereditary sensory autonomic neuropathies (HSAN) are rare forms of chronic neuropathies in children,...
Hereditary sensory and autonomic neuropathy type V (HSAN V) is an autosomal recessive disorder chara...
How to Cite This Article: Azadvari M, Emami Razavi SZ, Kazemi Sh. Hereditary Sensory and Autonomic N...
Hereditary Sensory and Autonomic Neuropathy (HSAN) is a rare group of diseases involving varying deg...
Hereditary Sensory Autonomic Neuropathy II (HSAN II) is a rare genetic disorder, characterized by se...