IN THE LEFT SIDE OF THE FACE, BLURRED VISION IN THE LEFT EYE IN NIGHTS ANAMNESIS AND EXAMINATION: THE PATIENT INDICATED THAT HE WAS SUFFERING FROM ANHYDROSIS
IN THE LEFT SIDE OF THE FACE AND BLURRED VISION IN THE LEFT EYE IN NIGHTS SINCE HE WAS A CHILD AND HE WAS DIAGNOSED AS HAVING HORNER'S SYNDROME.
Other signs for the involvement of the sympathetic chain were assessed with the presence of ptosis, anhydrosis
All the OPP patients were treated with repeated doses of intravenous bolus of 2mg atropine after every 10-15 minutes to achieve tachycardia, xerostomia, mydriasis, flushing and anhydrosis
. The OPP patients were then maintained with continuous infusion of atropine 1mg/h according to the features of adequate atropinization such as dry mouth, dry flushed skin, dry tongue, rapid heart rate (120-140/min) and noticeable dilation of pupils.
Additionally, there are effective treatments for common internal medicine problems such as EMS, PPID, anhydrosis
, and many others.
The causes of Charcot hip joint include tabes dorsalis, syringomyelia, peripheral nerve injury due to diabetes mellitus, and congenital insensivity to pain with anhydrosis
. Charcot arthropathy caused by these diseases has long been considered an absolute contraindication for total hip arthroplasty (THA) .
Neurological Manifestations in Different types of Leprosy Patients Neurological LL BL BT TT PN Total Manifestations Cranial nerves affected Trigeminal nerve 1 3 2 6 Facial nerve 3 3 Muscular system Disability claw hands 2 2 1 5 Flexion deformity of toes 1 1 2 Muscles wasting Upper limbs 2 2 1 5 Lower limbs 1 1 3 5 Sensory system Superficial sensation Mononeuropathy 11 4 15 Ulnar side Radial side 2 2 1 5 Glove and stock 1 anaesthesia Maculo-anaesthetic 1 7 30 38 Trophic and vasomotor changes anhydrosis
4 12 20 Cranial Nerves
Congenital insensitivity to pain and anhydrosis
: diagnostic and therapeutic dilemmas revisited.
The neurologist determined that JJ had small fiber neuropathy with anhydrosis
, suggestive of idiopathic erythromelalgia.
The typical clinical features include myosis, ipsilateral blepharoptosis, enophthalmos, facial anhydrosis
, and vascular dilation of the lateral part of the face.
HSAN type 4 demonstrates autosomal recessive transmission pattern, with such major characteristics as loss of sense of pain, self-mutilation, anhydrosis
and mental retardation.
Congenital insensitivity to pain with anhydrosis
(CIPA) is a rare genetic disorder characterized by inability to feel pain and temperature, and decreased or absent sweating.