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1,332 Possible Causes for Cerebellar Hypoplasia, Irritability, Weakness

  • Arnold Chiari Malformation

    We report a rare case of acute respiratory failure in a previously asymptomatic patient showing clinical signs of inferior cranial nerve palsy together with weakness and muscular[] Symptoms of Chiari in babies and children may vary somewhat and can include: Feeding problems including swallowing difficulties, excessive drooling, gagging, vomiting and irritability[] Type IV is a form a cerebellar hypoplasia.[]

  • Adult Krabbe Disease

    , hypotonia, megalencephaly, psychomotor retardation, loss of vision, abnormal MRI – 0.03 75 p.I250T (c.749T C)/p.I250T (c.749T C) 9 F 4.5 months 6.5 months Irritability,[] Hypoplasia (LCH), Polymicrogyria (PMG), Schizencephaly (SCH), Muscle-Eye-Brain (MEB) Disease, and Walker-Warburg syndrome (WWS), 17p13.3 deletion] Liver conditions (biliary[] , megalencephaly, CSF protein level – 0.0 434 c.1161 6532_polyA 9kbdel/c.1161 6532_polyA 9kbdel hom p.R184C ( c.550C T ) 2 M Unknown 4 months Seizures, irritability, feeding[]

  • Cervical Radiculitis

    The disc material itself is very acidic and causes a chemical burn or irritation to the surrounding tissue.[] Remember that radiculopathy weakness means the nerve is not stimulating the muscle properly. Weakness is not because you are not exercising enough.[] hypoplasia and hydranencephaly multiple chemical sensitivity multiple congenital anomalies-hypotonia-seizures syndrome Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual[]

  • Pilocytic Astrocytoma

    […] postulated hypotheses of viral-induced or angiogenic factor-induced glial growth, we hypothesize that neoplastic origins of hypothalamic-optochiasmatic glioma might be due to the irritative[] We present the case of a 2-year-old boy with progressive left-sided weakness and a cranial magnetic resonance imaging (MRI) scan showing a lesion with a cystic component in[] He also had a deep wider peduncular fossa, thickened superior cerebellar peduncle, and inferior vermian hypoplasia along with optochiasmatic tumor.[]

  • Autosomal Recessive Parkinson Disease 14

    These peripheral nerve problems include weakness and problems with sensation.[] QT SYNDROME 4 CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED Ataxin-1 (N76/3, N76/8) SPINOCEREBELLAR ATAXIA 1 CASK (K56A/50) MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR[] Symptoms of SCA People with SCA have symptoms of anemia, including fatigue, weakness, fainting, and palpitations or an increased awareness of their heartbeat.[]

  • Arnold-Chiari Malformation Type 1

    These can include arm and shoulder weakness, soreness or other sensory symptoms, low energy levels, lower cranial nerve dysfunction (impaired gag reflex, facial weakness or[] Symptoms in infants Symptoms in infants from any type of CM may include: trouble swallowing irritability when eating excessive drooling gagging or vomiting irregular breathing[] hypoplasia without displacement of the cerebellum through the foramen magnum probably a variation of cerebellar hypoplasia Chiari V malformation absent cerebellum herniation[]

  • Dandy-Walker Syndrome

    Marinesco-Sjögren syndrome (MSS) is a rare autosomal recessive disorder, which is characterized by congenital cataracts, cerebellar ataxia, progressive muscle weakness, and[] They may also show symptoms of increased intracranial pressure due to hydrocephalus, and these include irritability, vomiting and convulsions.[] hypoplasia, hydrocephalus, and posterior fossa cyst formation.[]

  • Cervical Spondylosis

    This symptom is caused by irritation of a spinal nerve as it leaves the bony (vertebral) area.[] We found 19 patients with weakness and atrophy of the intrinsic hand muscles, and 13 patients with weakness proximal to the hand muscles to serve as a control group.[] Angiography showed two extracranial right vertebral artery (VA) stenoses, left VA hypoplasia, absence of left PICA and a dominant right PICA.[]

  • Amish Lethal Microcephaly

    The severity and pattern of muscle weakness varies, but most affected individuals show mildly delayed motor development, hypotonia, generalized muscle weakness, and weakness[] Irritable 0000737 Metabolic acidosis 0001942 Microcephaly Abnormally small skull Decreased circumference of cranium Decreased size of skull Reduced head circumference Small[] The single affected individual described by Siu et al [2010] had irritability and profound developmental delay.[]

  • Congenital Merosin-Positive Muscular Dystrophy

    Overview A very rare group of diseases that involves early infantile onset of muscle weakness, loss of muscle tone and contractures.[] From the 1 st month of life, the patient was hypotonic with poor intake, irritability, reduced spontaneous movements, and poor suction.[] The second child, a 3-year-old ambulant girl with subtle learning problems, had mild cerebellar hypoplasia and a large subarachnoid space when scanned at 16 months.[]

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