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Hereditary sensory and autonomic neuropathy

Index Hereditary sensory and autonomic neuropathy

Hereditary sensory and autonomic neuropathy (HSAN) or hereditary sensory neuropathy (HSN) is a condition used to describe any of the types of this disease which inhibit sensation. [1]

16 relations: Autoamputation, Charcot–Marie–Tooth disease, Congenital insensitivity to pain with anhidrosis, DNMT1, Dominance (genetics), Familial dysautonomia, HSN2, Hypohidrosis, IKBKAP, Morvan's syndrome, Nerve conduction velocity, Nerve growth factor, Peripheral nervous system, RAB7A, SPTLC1, Tropomyosin receptor kinase A.

Autoamputation

Autoamputation is the spontaneous detachment (amputation) of an appendage from the body.

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Charcot–Marie–Tooth disease

Charcot–Marie–Tooth disease (CMT) is one of the hereditary motor and sensory neuropathies, a group of varied inherited disorders of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body.

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Congenital insensitivity to pain with anhidrosis

Congenital insensitivity to pain with anhidrosis (CIPA), also called hereditary sensory and autonomic neuropathy type IV, is an extremely rare inherited disorder of the nervous system which prevents the sensation of pain, heat, cold, or any real nerve-related sensations (including feeling the need to urinate); however, patients can still feel pressure.

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DNMT1

DNA (cytosine-5)-methyltransferase 1 is an enzyme that catalyzes the transfer of methyl groups to specific CpG structures in DNA, a process called DNA methylation.

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Dominance (genetics)

Dominance in genetics is a relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus.

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Familial dysautonomia

Familial dysautonomia (FD), sometimes called Riley–Day syndrome and hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory, sympathetic and some parasympathetic neurons in the autonomic and sensory nervous system resulting in variable symptoms, including insensitivity to pain, inability to produce tears, poor growth, and labile blood pressure (episodic hypertension and postural hypotension).

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HSN2

Hereditary sensory neuropathy, type II also known as HSN2 is a protein which in humans in encoded by the HSN2.

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Hypohidrosis

Hypohidrosis is diminished sweating in response to appropriate stimuli.

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IKBKAP

IKBKAP (inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein) is a human gene encoding the IKAP protein, which is ubiquitously expressed at varying levels in all tissue types, including brain cells.

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Morvan's syndrome

Morvan's syndrome, or Morvan's fibrillary chorea (MFC), is a rare autoimmune disease named after the nineteenth century French physician Augustin Marie Morvan.

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Nerve conduction velocity

Nerve conduction velocity is an important aspect of nerve conduction studies.

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Nerve growth factor

Nerve growth factor (NGF) is a neurotrophic factor and neuropeptide primarily involved in the regulation of growth, maintenance, proliferation, and survival of certain target neurons.

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Peripheral nervous system

The peripheral nervous system (PNS) is one of the two components of the nervous system, the other part is the central nervous system (CNS).

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RAB7A

Ras-related protein Rab-7a is a protein that in humans is encoded by the RAB7A gene.

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SPTLC1

Serine palmitoyltransferase, long chain base subunit 1, also known as SPTLC1, is a protein which in humans is encoded by the SPTLC1 gene.

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Tropomyosin receptor kinase A

Tropomyosin receptor kinase A (TrkA), also known as high affinity nerve growth factor receptor, neurotrophic tyrosine kinase receptor type 1, or TRK1-transforming tyrosine kinase protein is a protein that in humans is encoded by the NTRK1 gene.

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Redirects here:

Congenital Sensory Neuropathy, Congenital insensitivity to pain with partial anhidrosis, Congenital sensory neuropathy, Familial syringomyelia, Familial trophoneurosis, HSAN, HSAN I, HSAN II, HSAN Type 1, HSAN Type 2, HSAN Type 5, HSAN Type I, HSAN Type II, HSAN Type V, HSAN V, HSAN type 1, HSAN type 2, HSAN type 5, HSAN type I, HSAN type II, HSAN type V, HSAN-1, HSAN-2, HSAN-5, HSAN-I, HSAN-II, HSAN-V, HSAN1, HSAN2, HSAN5, Hereditary Sensory Autonomic Neuropathy, Hereditary Sensory Radicular Neuropathy, Hereditary sensory and autonomic neuropathies, Hereditary sensory and autonomic neuropathy type 1, Hereditary sensory and autonomic neuropathy type 2, Hereditary sensory and autonomic neuropathy type 5, Hereditary sensory neuropathies, Hereditary sensory neuropathy, Hereditary sensory radicular neuropathy, Inability to feel pain, Insensitivity to pain, Mal perforant du pied, Pain insensitivity, Thevenard syndrome, Ulcero-mutilating neuropathy.

References

[1] https://en.wikipedia.org/wiki/Hereditary_sensory_and_autonomic_neuropathy

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