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167 Possible Causes for Poor Feeding, primarily in the legs, severe muscle wasting

Did you mean: Poor Feeding, primarily in the legs, severe, muscle wasting

  • Spinal Muscular Atrophy

    […] diagnosis of infants with congenital contractures and severe muscle weakness by wasting mainly confined to the upper limbs.[ncbi.nlm.nih.gov] feeding, abnormal postures and scoliosis, loss of joint range of motion, abnormal movement or walking patterns, and respiratory problems.[moveforwardpt.com] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org]

  • Spinal Muscular Atrophy Type 1

    atrophy type 1 with paradoxical breathing were placed on high-span PIP PEEP when sleeping from the point of diagnosis of spinal muscular atrophy.[ncbi.nlm.nih.gov] Poor sucking ability and reduced swallowing are frequent, leading to feeding difficulties. Deep tendon reflexes are absent. Respiratory failure is common.[orpha.net] This form affects primarily the muscles in the legs.[mda.org]

  • Distal Spinal Muscular Atrophy Type 3

    Characterised by severe muscle wasting as in SMA type I accompanied by congenital bone fractures PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) Pontocerebellar[ipfs.io] feeding, abnormal postures and scoliosis, loss of joint range of motion, abnormal movement or walking patterns, and respiratory problems.[moveforwardpt.com] This form affects primarily the muscles in the legs.[mda.org]

  • Muscular Atrophy

    Neuromyopathy associated ketosis should be considered in all patients with severe muscle wasting presenting with an elevated anion gap metabolic ketoacidosis.[ncbi.nlm.nih.gov] feeding, abnormal postures and scoliosis, loss of joint range of motion, abnormal movement or walking patterns, and respiratory problems.[moveforwardpt.com] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Characterised by severe muscle wasting as in SMA type I accompanied by congenital bone fractures PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) Pontocerebellar[ipfs.io] difficulties -May require G-tube for feeding -Muscle fasciculations - inc tongue -Tremor may be present -In general, alert and responsive What is type 1 SMA known as?[quizlet.com] This form affects primarily the muscles in the legs.[mda.org]

  • Spinal Muscular Atrophy Type 3

    SMA type IV is the least severe type of the disease where weakness and muscle wasting generally start in adulthood.[stemcellthailand.org] They include severe weakness or 'floppiness', poor head control, weak cry and cough, and difficulty with swallowing and feeding.[rch.org.au] This form affects primarily the muscles in the legs.[mda.org]

  • Adult Spinal Muscular Atrophy

    […] spinal muscular atrophy and juvenile asymmetric segmental spinal muscular atrophy.[symptoma.com] Symptoms in an infant: Breathing difficulty, leading to a lack of oxygen Feeding difficulty (food may go into the windpipe instead of the stomach) Floppy infant (poor muscle[medlineplus.gov] The condition primarily affects the muscles that control chewing and swallowing, chest wall muscles, and arm and leg muscles.[ucsfbenioffchildrens.org]

  • Muscular Dystrophy-Dystroglycanopathy Type B5

    Spinal Muscular Atrophy type 1, Werdnig-Hoffmann Disease. Spinal Muscular Atrophy type 2. Spinal Muscular Atrophy type 3, Kugelberg-Welander Disease.[terkko.helsinki.fi] Interventions may be needed for inadequate weight gain and poor feeding.[ncbi.nlm.nih.gov] This form affects primarily the muscles in the legs.[mda.org]

  • Mandibulofacial Dysostosis

    ., our lab specializes in molecular diagnosis of neuromuscular diseases including muscular dystrophy, spinal muscular atrophy, Emery Dreifuss muscular dystrophy and Pelizaeus-Merzbacher[nemours.org] MFDM is caused by mutations in the EFTUD2 gene and is inherited in an autosomal dominant manner. 0000750 Feeding difficulties Feeding problems Poor feeding Last updated: 7[rarediseases.info.nih.gov] [acro- dysostosis] Acrodysostosis An autosomal dominant condition which primarily affects bone and is characterised by ocular hypertelorism, brachycephaly, small upturned[medical-dictionary.thefreedictionary.com]

  • Distal Hereditary Motor Neuropathy

    feeding, esophageal dysmotility ,vomiting ,recuurent fever & chest infection) Emotional stimuli provoke episodic hypertension, profuse sweating &marked skin blotching due[slideshare.net] It results in muscle weakness and affects movement, primarily in the legs.[ghr.nlm.nih.gov] Neurological examination revealed a symmetrical severe muscle wasting and weakness in distal lower and upper limbs, with claw hands, footdrop with equinovarus deformity and[ncbi.nlm.nih.gov]

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