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15 Possible Causes for Favism, Lathyrism

  • Favism

    Favism is most commonly diagnosed in children between 1-5 years of age with G6PD, while cases of favism in adults have been infrequently reported.[symptoma.com] The reader is also introduced to lathyrism, the toxicity of agglutinins, occurrence of goitrogens in thioglucoside-containing plants, and dietary sources of cyanogen.[books.google.de] Pathophysiology of favism, including incidence, salient features, and sequence of events. 2.[ncbi.nlm.nih.gov]

  • Rheum Rhaponicum Poisoning

    المحددة صفحة العنوان جدول المحتويات فهرس المراجع المحتويات Introduction 1 Estrogens in Foods 18 Tumorigenic and Carcinogenic Natural Products 24 Lathyrogens in Foods 40 Favism[books.google.com] […] goitrogenic Gossypol growth hemagglutinin high levels human hypertension Hypervitaminosis immunological increased infants ingestion inhibit intake intestinal iodine isolated Lathyrism[books.google.com] […] clinical components compounds Cottonseed Meal Cow's Milk deficiency diet containing dietary disease doses enzyme ergot Estrogens excess experimental Exptl extracts factor Favism[books.google.com]

  • Hypervitaminosis E

    المحددة صفحة العنوان جدول المحتويات فهرس المراجع المحتويات Introduction 1 Estrogens in Foods 18 Tumorigenic and Carcinogenic Natural Products 24 Lathyrogens in Foods 40 Favism[books.google.com] […] goitrogenic Gossypol growth hemagglutinin high levels human hypertension Hypervitaminosis immunological increased infants ingestion inhibit intake intestinal iodine isolated Lathyrism[books.google.com] […] clinical components compounds Cottonseed Meal Cow's Milk deficiency diet containing dietary disease doses enzyme ergot Estrogens excess experimental Exptl extracts factor Favism[books.google.com]

  • Primaquine

    History of favism.[empr.com] The reader is also introduced to lathyrism, the toxicity of agglutinins, occurrence of goitrogens in thioglucoside-containing plants, and dietary sources of cyanogen.[books.google.ro]

  • Autosomal Dominant Spastic Paraplegia Type 13

    […] congenital 4, autosomal recessive 612541 611045 Autosomal recessive G6PC3 17q21.31 Dursun syndrome 612541 611045 Autosomal recessive G6PD Xq28 Hemolytic anemia, G6PD deficient (favism[mnglabs.com] Two other disorders with spastic paraplegia symptoms termed Lathyrism and Konzo are caused by toxins in the plants Lathyrus sativus and cassava.[sp-foundationorg.presencehost.net] (myelitis) Dural arteriovenous malformation Chiari malformation Adrenoleucodystrophy Hereditary spastic paraplegia Spinocerebellar ataxias Vitamin defi ciency (B12 and E) Lathyrism[slideshare.net]

  • X-Linked Spastic Paraplegia Type 34

    […] congenital 4, autosomal recessive 612541 611045 Autosomal recessive G6PC3 17q21.31 Dursun syndrome 612541 611045 Autosomal recessive G6PD Xq28 Hemolytic anemia, G6PD deficient (favism[mnglabs.com] (myelitis) Dural arteriovenous malformation Chiari malformation Adrenoleucodystrophy Hereditary spastic paraplegia Spinocerebellar ataxias Vitamin defi ciency (B12 and E) Lathyrism[slideshare.net]

  • Autosomal Recessive Spastic Paraplegia Type 18

    […] congenital 4, autosomal recessive 612541 611045 Autosomal recessive G6PC3 17q21.31 Dursun syndrome 612541 611045 Autosomal recessive G6PD Xq28 Hemolytic anemia, G6PD deficient (favism[mnglabs.com] (myelitis) Dural arteriovenous malformation Chiari malformation Adrenoleucodystrophy Hereditary spastic paraplegia Spinocerebellar ataxias Vitamin defi ciency (B12 and E) Lathyrism[slideshare.net]

  • Spastic Paraplegia - Ataxia - Mental Retardation

    17q21.31 Dursun syndrome 612541 611045 Autosomal recessive G6PD Xq28 {Resistance to malaria due to G6PD deficiency} 611162 305900 G6PD Xq28 Hemolytic anemia, G6PD deficient (favism[mnglabs.com] Two other disorders with spastic paraplegia symptoms termed Lathyrism and Konzo are caused by toxins in the plants Lathyrus sativus and cassava.[sp-foundationorg.presencehost.net] Muscle spasticity and weakness can also be caused by other conditions including (but not limited to) Tropical Spastic Paraparesis and conditions called Lathyrism and Konzo[sp-foundationorg.presencehost.net]

  • Autosomal Dominant Spastic Paraplegia Type 19

    17q21.31 Dursun syndrome 612541 611045 Autosomal recessive G6PD Xq28 {Resistance to malaria due to G6PD deficiency} 611162 305900 G6PD Xq28 Hemolytic anemia, G6PD deficient (favism[mnglabs.com] (myelitis) Dural arteriovenous malformation Chiari malformation Adrenoleucodystrophy Hereditary spastic paraplegia Spinocerebellar ataxias Vitamin defi ciency (B12 and E) Lathyrism[slideshare.net]

  • Autosomal Dominant Spastic Paraplegia Type 37

    […] congenital 4, autosomal recessive 612541 611045 Autosomal recessive G6PC3 17q21.31 Dursun syndrome 612541 611045 Autosomal recessive G6PD Xq28 Hemolytic anemia, G6PD deficient (favism[mnglabs.com] (myelitis) Dural arteriovenous malformation Chiari malformation Adrenoleucodystrophy Hereditary spastic paraplegia Spinocerebellar ataxias Vitamin defi ciency (B12 and E) Lathyrism[slideshare.net]

Further symptoms