A case of miliaria profunda after excessive sweating during a summer vacation
We present the case of an otherwise healthy 34‐year‐old man of Asian descent diagnosed with miliaria profunda after a 6‐week history of generalised anhidrosis after a trip to Mallorca in the summer.
Ariana Palacio +5 more
doaj +1 more source
Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient
Congenital insensitivity to pain with anhidrosis is a rare disease of the nervous system which causes one to lose their feeling of pain. The disease is subtype four of hereditary sensory and autonomic neuropathy (HSAN IV) that results from NTRK1 gene ...
Marzye Mohammadi-Anaie +1 more
core
Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder presenting with loss of pain sensation, thermal sensation defects, and self-mutilating behavior.
Husna Zayadi
core +1 more source
Silent Suffering: Congenital Insensitivity to Pain With Anhidrosis in a Single Family. [PDF]
Alshehri A +5 more
europepmc +1 more source
Additional Evidence Fails to Associate Variation in KCNE4 With Equine Anhidrosis. [PDF]
Petersen JL, Finno CJ.
europepmc +1 more source
Brown-Séquard syndrome caused by cervical disc herniation with associated Horner's syndrome: a case report. [PDF]
Park GJ, Kwon DY, Kim KR.
europepmc +1 more source
Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis [PDF]
application/pdf論文(Article)Congenital insensitivity to pain with anhidrosis (CIPA; MIM 256800) is an autosomal-recessive disorder characterized by recurrent episodes of unexplained fever, anhidrosis (absence of sweating) and absence of reaction to noxious
Matsuda, Ichiro +24 more
core
Considerations in Restorative Management and New Oral Findings in a Patient With Congenital Insensitivity to Pain With Anhidrosis. [PDF]
Chay PL +6 more
europepmc +1 more source
Congenital sensory neuropathy with anhidrosis (hereditary sensory neuropathy type IV)
Hereditary sensory neuropathies comprise a group of rare childhood diseases which are classified into four types. We present a Greek boy 11 years old with hereditary sensory neuropathy type IV (congenital sensory neuropathy with anhidrosis) whom we have ...
Gourgiotou, K. +5 more
core
Partial Horner's Syndrome Following Thyroidectomy Without Lateral Neck Dissection: A Rare Case Report and Literature Review. [PDF]
Hopping E, Ayeni FE, Edirimanne S.
europepmc +1 more source

