Abstract Background Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder characterized by hyperpyrexia, anhidrosis, pain insensitivity, self-inflicted injuries, and intellectual disability. The anesthetic management of these patients is challenging owing to the high risk of perioperative complications resulting from their autonomic dysfunction, such as hyperthermia, hypotension, and bradycardia, which result from autonomic nervous system dysfunction. Case presentation Two 3-year-old Han Chinese identical male twins (weighing 13.5 kg and measuring 93 cm tall) were previously diagnosed as having congenital insensitivity to pain with anhidrosis based on clinical features and genetic screening. According to th...
Background: Familial Dysautonomia (FD) is a rare hereditary syndrome which is an autosomal recessive...
Introduction: Tamsulosin, a selective alpha1-adrenergic receptor (alpha1-AR) antagonist, is a widely...
Septo-optic dysplasia (SOD)/de Morsier's syndrome is characterized by optic nerve hypoplasia, pituit...
SummaryBackground and objectivesCongenital insensitivity to pain and Anhidrosis (CIPA) or hereditary...
Congenital insensitivity to pain syndrome is a rare, sensorial and autonomic neuropathy characterize...
Hereditary sensory autonomic neuropathy type IV is a rare disorder with an autosomal recessive trans...
Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classifie...
A patient with congenital insensitivity to pain with anhidrosis (CIPA) underwent revision of total h...
PURPOSE: To report the perioperative management of anesthesia and analgesia in a child presenting wi...
AbstractEctodermal dysplasias are rare conditions with a triad of hypotrichosis, anodontia and anhid...
Anesthesiafor a child with Menkes syndromePurpose/aim:Menkes syndrome is an X-linked recessively inh...
Congenital insensitivity to pain (CIP) is a rarely syndrome and is characterized by unresponsiveness...
ABSTRACT Ectodermal dysplasias are rare conditions with a triad of hypotrichosis, anodontia and anhi...
Summary points - Congenital insensitivity to pain is a rare autosomal recessive disease characteriz...
Anaesthesia management of the conjoined twins poses some difficulties both for the anaesthesiologist...
Background: Familial Dysautonomia (FD) is a rare hereditary syndrome which is an autosomal recessive...
Introduction: Tamsulosin, a selective alpha1-adrenergic receptor (alpha1-AR) antagonist, is a widely...
Septo-optic dysplasia (SOD)/de Morsier's syndrome is characterized by optic nerve hypoplasia, pituit...
SummaryBackground and objectivesCongenital insensitivity to pain and Anhidrosis (CIPA) or hereditary...
Congenital insensitivity to pain syndrome is a rare, sensorial and autonomic neuropathy characterize...
Hereditary sensory autonomic neuropathy type IV is a rare disorder with an autosomal recessive trans...
Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classifie...
A patient with congenital insensitivity to pain with anhidrosis (CIPA) underwent revision of total h...
PURPOSE: To report the perioperative management of anesthesia and analgesia in a child presenting wi...
AbstractEctodermal dysplasias are rare conditions with a triad of hypotrichosis, anodontia and anhid...
Anesthesiafor a child with Menkes syndromePurpose/aim:Menkes syndrome is an X-linked recessively inh...
Congenital insensitivity to pain (CIP) is a rarely syndrome and is characterized by unresponsiveness...
ABSTRACT Ectodermal dysplasias are rare conditions with a triad of hypotrichosis, anodontia and anhi...
Summary points - Congenital insensitivity to pain is a rare autosomal recessive disease characteriz...
Anaesthesia management of the conjoined twins poses some difficulties both for the anaesthesiologist...
Background: Familial Dysautonomia (FD) is a rare hereditary syndrome which is an autosomal recessive...
Introduction: Tamsulosin, a selective alpha1-adrenergic receptor (alpha1-AR) antagonist, is a widely...
Septo-optic dysplasia (SOD)/de Morsier's syndrome is characterized by optic nerve hypoplasia, pituit...