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61 Possible Causes for Cafe-Au-Lait Spots, Generalized Motor Seizure, Pallor

  • Pheochromocytoma

    The subject should be examined for cafe au lait spots if neurofibromatosis is suspected.[] BACKGROUND: Pheochromocytoma is an endocrine tumor that causes hypertension, facial pallor, and headache.[] The following common presenting signs and symptoms are seen in patients diagnosed with pheochromocytoma: Elevated blood pressure Severe headache Tremors Tachypnea Pallor of[]

  • Tuberous Sclerosis

    Additional skin lesions may also develop, including cafe-au-lait spots; fibromas (benign, fibrous nodules) arising around or beneath the nails; or shagreen patches (rough,[] Differentials to exclude: Neurofibromatosis type 1: Cafe au lait spots, neurofibromas, axillary freckling, lisch nodules.[] These are known as cafe-au-lait spots. A child may also have skin tumors that are not cancer (benign). These are called neurofibromas.[]

  • Polycythemia Neonatorum

    au lait spots - suspect neurofibromatosis if there are many large spots.[] Continue reading RHESUS DISEASE Haemolytic anaemia in neonatal period is typified by rhesus disease in which there is rapid onset of jaundice within first 24 hours with pallor[] Pallor Anemia Hepatosplenomegaly Extravascular hemolysis occurs in the spleen and liver, which sequesters damaged RBCs.[]

  • Generalized Clonic or Tonic-Clonic Seizures

    Plagiocephaly Athetosis Sarcoma Abnormal lung lobation Abnormality of the upper limb Duodenal atresia Acute leukemia Multiple renal cysts Abnormality of the skull Multiple cafe-au-lait[] TONIC-CLONIC SEIZURE AND VARIANTS Generalized tonic-clonic seizures are bilateral and symmetric generalized motor seizures, that occur in an individual with loss of consciousness[] Seizures of Generalized Onset Grand mal (generalized motor) Generalized seizures involve abnormal electrical activity in all of the cerebral cortex simultaneously.[]

  • Ring Chromosome 11 Syndrome

    Ring chromosome 11 and cafe-au-lait spots . American Journal of Medical Genetics 30 911–916. 10.1002/ajmg.1320300406 [ PubMed ] [ CrossRef ] [ Google Scholar ] 9.[] The majority of the patients experienced more than one seizure type, including complex partial seizures, atypical absences, generalized tonic-clonic seizures and focal motor[] Case Report A 71 years elderly was presented with a history of weakness/fatigability/exertional breathlessness/fever/jaundice/progressive pallor/wet purpura/petechial spots[]

  • Schwartz-Lelek Syndrome

    au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… … Wikipedia ANKH — Ankylosis, progressive homolog (mouse), also known as ANKH[] Flat face Cortical visual impairment Cerebral atrophy Congenital nephrotic syndrome Subependymal nodules Generalized hypotonia Motor delay Myopathy Diaphyseal thickening[] Evolving disc pallor and nystagmus prompted bilateral optic nerve decompression and bifrontal craniectomy at the age of 21 months and, in view of restenosis of the optic canals[]

  • Phakomatosis Pigmentokeratotica

    Hyperpigmented macules may be seen in NF1 & NF2 (cafe-au-lait spots), tuberous sclerosis (cafe-au-lait spots), and incontinentia pigmenti ("splashed paint" spots).[] The morphology of the seizures varies from infantile spasms or focal motor seizures to generalized tonic or tonic-clonic seizures.[] Angiokeratoma of Mibelli Angiokeratoma of Fordyce (scrotal angiokeratoma) Angiokeratoma Circumscriptum Solitary Papular angiokeratoma Angiokeratoma Corporis Diffusum T/F peripheral pallor[]

  • Patterson Pseudoleprechaunism Syndrome

    […] group G - cafe au lait spots Fanconi's anemia -- Complementation group I - cafe au lait spots Fanconi's anemia -- Complementation group J - cafe au lait spots Fanconi's anemia[] […] delay Small for gestational age Synophrys Prominent nasal bridge Abnormality of the pinna Generalized myoclonic seizures Intellectual disability, progressive Autosomal dominant[] […] skin Ectodermal dysplasia Hypopigmentation of the skin Hypodontia Immunodeficiency Abnormality of skin pigmentation Retinal detachment Papule Malabsorption Nail dystrophy Pallor[]

  • Helsmoortel-van der Aa Syndrome

    Generalized lentiginosis is characteristic but they may not be present until age 4 or 5 years following the appearance of cafe-au-lait spots.[] motor seizures; polyneuropathy; genetic testing available SCA11 (autosomal dominant type 11) 15q14-q21.3 by linkage Slowly progressive gait and extremity ataxia, dysarthria[] (A) Eye fundus (RE: right eye; LE: left eye) from patient II.4 (top) and patient III.4 (bottom) disclose temporal pallor of the optic disks.[]

  • Spastic Ataxia with Congenital Miosis

    […] and mid-face are extremely tender to light palpation Cavernous sinus thrombosis (involves CN III, IV, V, and VI which all travel through cavernous sinus) 1 year old with cafe-au-lait[] […] hereditary optic atrophy, seen in only 4 families to date, with an onset in early childhood, characterized by progressive loss of visual acuity, significant optic nerve pallor[] Optic disc changes are an increase in the diameter and depth of the physiological cup and increased pallor.[]

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