neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2
neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 is a medical condition that may be associated with various symptoms and signs.
Also known as: IMNEPD2.
Category: General
Symptoms associated with neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2
The following symptoms have been associated with neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 in medical literature. Not everyone experiences the same symptoms.
Bilateral sensorineural hearing impairment
A form of sensorineural hearing impairment that affects both ears....
Deeply set eye
An eye that is more deeply recessed into the plane of the face than is typical....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Generalized-onset seizure
A generalized-onset seizure is a type of seizure originating at some point within, and rapidly engaging, bilat...
Prolonged neonatal jaundice
Neonatal jaundice refers to a yellowing of the skin and other tissues of a newborn infant as a result of incre...
Vomiting
Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic...
Weakness of facial musculature
Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve)....
Tests used to investigate neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2
Healthcare providers may order these tests when evaluating neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2. Test selection is a clinical decision made by a qualified professional.
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Conditions with overlapping symptoms
These conditions share symptoms with neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2, which is why a clinical evaluation is important.
Houge-Janssens syndrome 4
Houge-Janssens syndrome 4 is a medical condition that may be associated with various symptoms and signs....
Melnick-Needles syndrome
A otopalatodigital syndrome spectrum disorder and is associated with a short stature, facial dysmorphism, osse...
Morimoto-Ryu-Malicdan neuromuscular syndrome
Morimoto-Ryu-Malicdan neuromuscular syndrome is a medical condition that may be associated with various sympto...
RNU5B-1 related neurodevelopmental disorder with seizures and joint laxity
A neurodevelopmental disorder in which the cause of the disease is a variation in RNU5B-1 gene and is characte...
developmental delay, impaired speech, and behavioral abnormalities
developmental delay, impaired speech, and behavioral abnormalities is a medical condition that may be associat...
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
mitochondrial DNA depletion syndrome 6 (hepatocerebral type) is a medical condition that may be associated wit...
Frequently Asked Questions
What is neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2?
neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 is a health condition described in medical literature. neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2?
neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 is associated with 7 symptoms in the medical literature we index, including Bilateral sensorineural hearing impairment, Deeply set eye, Failure to thrive, Generalized-onset seizure, Prolonged neonatal jaundice, Vomiting. Symptoms vary widely between individuals.
How is neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2 include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.
Is SymptomDatabase.com diagnosing me?
No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2, please discuss your symptoms with a qualified healthcare provider.