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68 Possible Causes for Cranial Nerve Palsy, Early Onset Puberty, X-Ray Abnormal

  • Diabetes Mellitus

    Type 1 DM usually starts in children aged 4 years or older, appearing fairly abruptly, with the peak incidence of onset at age 11-13 years (ie, in early adolescence and puberty[] Cranial neuropathies cause diplopia, ptosis, and anisocoria when they affect the 3rd cranial nerve or motor palsies when they affect the 4th or 6th cranial nerve.[] […] most often affect the proximal L2 through L4 nerve roots, causing pain, weakness, and atrophy of the lower extremities (diabetic amyotrophy), or the proximal T4 through T12 nerve[]

  • Porphyria

    Clinical onset usually occurs in infancy or in early childhood, but very rare cases of onset at puberty or later have been reported. [31] Hemolysis may be a feature in homozygous[] nerve palsies Confusion Coma Seizures Fever EXAMINATION as directed by history INVESTIGATIONS urinary porphyrins & porphyrin precursors (ALA and PBG) serum porphyrins faecal[] […] precipitants — drugs, stress, infection, alcohol, menstruation, pregnancy, starvation, dehydration Abdo pain Vomiting Motor and sensory neuropathy Autonomic dysfunction Cranial[]

  • Pulmonary Hemangioma

    In January 2003, a 73-year-old female presented with abnormal chest X-ray findings.[] onset of puberty.[] Other causes of ptosis include third cranial nerve palsy and neurological muscular disorders such as myasthenia and muscle dystrophies.[]

  • Autosomal Recessive Osteopetrosis Type 7

    Jaw growth stabilizes during puberty, and facial features improve and are normal in most adults with the disease. [113] Can affect the development of the teeth.[] Furthermore, excessive bone tends to obturate cranial nerve foramina and provoke cranial nerve palsy.[] nerves palsy - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding - Hypocalcemia - Hypophosphatemia - Pulmonary artery stenosis / absence / hypoplasia[]

  • Diabetic Autonomic Neuropathy

    In these people, the unusually dense bones may be discovered by accident when an x-ray is done for another reason.[] Type 1 DM usually starts in children aged 4 years or older, appearing fairly abruptly, with the peak incidence of onset at age 11-13 years (ie, in early adolescence and puberty[] Classification type I: pronounced osteosclerosis of cranial vault with clinical presentation as cranial nerve palsies type II: end plate thickening of vertebrae (sandwich[]

  • Spastic Ataxia with Congenital Miosis

    Frequently abnormal X ray spine(bony changes) Absent May be present Present 21.  Some specific signs and symptoms which helps in evaluating the level of spinal cord involvement[] Clinical features Early onset progressive ataxia Short stature Hypodontia Delayed puberty secondary to gonadal dysfunction Laboratory MRI shows white matter signal abnormalities[] Sixth nerve palsy was the most common (43%), and fourth cranial nerve palsy (15%) was the least common.[]

  • Suprasellar Tumor

    […] sella turcica x-ray.[] The high testosterone level in males inducing early onset of puberty, can be due to increased β-hCG.[] Cranial nerve palsy related to AC have been reported in isolated cases) [5-9].[]

  • Chiasmal Syndrome

    The characteristic presentation consisted of progressive impairment of vision without headache or abnormal plain skull x-ray films in patients with weight loss or diabetes[] Usually, the non-vision complications of extensive gliomas occur in infancy or early childhood, and onset of obstructive signs or hypothalamic involvement much beyond the[] Sneddon Syndrome Presenting With Unilateral Third Cranial Nerve Palsy Page Metadata Title Sneddon Syndrome Presenting With Unilateral Third Cranial Nerve Palsy Creator Jimnez-Gallo[]

  • Gastrointestinal Sarcoidosis

    Sarcoidosis is often found in patients who don't have any symptoms of sarcoidosis but who have abnormal chest X-ray results.[] Early onset childhood sarcoidosis Early onset childhood sarcoidosis (ie, with onset in the first 4 y of life) is a rare disease and appears to be different from sarcoidosis[] Patients may be free of chest symptoms despite an abnormal chest x-ray and biopsy-proven sarcoidosis.[]

  • Nelson Syndrome

    One already had cranial nerve abnormalities and visual field defects and had had both a craniotomy and deep x-ray treatment.[] The presented case seems to be an extreme phenotype of male 46, XY hypogonadism with a very early onset, left undiagnosed for 4 decades.[] nerve palsies are recognised complications.[]

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