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321 Possible Causes for Disturbance of Growth, Onset in Early Infancy

  • Progressive Familial Intrahepatic Cholestasis

    PFIC1 and PFIC2 manifest during infancy and progress to end-stage liver disease during early childhood, whereas the onset of PFIC3 is often delayed.[] Both patients had normal gamma-glutamyl transpeptidase levels, but showed severe pruritus with sleep disturbance, cholestasis, jaundice and growth failure.[] The age of onset can vary from infancy to adulthood, depending on the specific type of myoclonic epilepsy and the underlying genetic mutation.[]

  • Cryopyrin-Associated Periodic Syndrome

    […] is typically in infancy or early childhood.[] Children with CINCA may have growth disturbances during the course of the disease.[] It typically presents itself with a rash in early infancy. Similarly to MWS, fatigue is typically a symptom more frequently than fevers.[]

  • Early Infantile Epileptic Encephalopathy Type 6

    […] impediments Nutritional issues Sleep disturbances Chronic infections Sensory integration disorders Autonomic nervous system disruptions There is no cure for Dravet Syndrome[] From Wikidata Jump to navigation Jump to search epilepsy characterized by frequent febrile seizures and with onset before 1 year SMEI Severe myoclonic epilepsy in infancy[] Weakened immunity Growth and weight should also be followed closely and parents should be aware of treatment options such as gastrostomy tubes (g-tubes) when appropriate.[]

  • Congenital Disorder of Glycosylation Type 1I

    This severe autosomal recessive disease, often with onset in early infancy and impressive involvement of the CNS, was soon recognized as a multi-system disorder ( 5, 8 – 11[] She became oedematous with electrolyte disturbance within hours of birth and died 3 days later.[] This severe autosomal recessive disease, often with onset in early infancy and impressive involvement of the CNS, was soon recognized as a multi-system disorder ( 5 , 8 –[]

  • Benign Migratory Glossitis

    […] of symptoms occurs early in infancy and the patients are severely anemic and have a short life expectancy.[] Inhalt DISTURBANCES OF DEVELOPMENT AND GROWTH 1 S Tumors of the Salivary Glands 219 Cysts and Tumors of Odontogenic Origin 254 Section II 309 Viral Infections of the Oral[] […] and southern Italy. [33] The homozygous form of β-thalassaemia (thalassaemia major) exhibits the most severe clinical symptoms with marked orofacial deformities. [33] The onset[]

  • Vomiting of Pregnancy

    Appear in both sexes; onset in early infancy. Autosomal recessive inheritance is probable. First described by Brandt in 1936.[] Weight loss, dehydration, acidosis from malnutrition, alkalosis from vomiting, hypokalaemia, muscle weakness, electrocardiographic abnormalities, tetany, and psychological disturbances[] […] oesophageal rupture due to severe vomiting, Wernicke's encephalopathy, central pontine myelinolysis, retinal haemorrhage, renal damage, spontaneous pneumomediastinum, intrauterine growth[]

  • Cystinosis

    It commonly presents in early infancy with Fanconi syndrome, which consists of multiple defects in renal proximal tubular reabsorption.[] Growth retardation improved after correction of electrolyte disturbances, the initiation of cysteamine therapy and treatment with recombinant human growth hormone.[] Clinically the disorder shows a slowly progressive glomerular insufficiency rather than the prominent Fanconi syndrome, electrolyte and water disturbances, growth arrest,[]

  • Otitis Media

    infancy and childhood.[] In the worst case, the enlarging cholesteatoma (a growth of keratinizing squamous epithelium) "eats" the bony boundary of the cranial fossa, leading to meningitis, encephalitis[] […] of the TM into the middle ear Retraction: formation of an expansive retraction pouch due to a functional disturbance of the tube with loss of self-cleaning mechanism; development[]

  • Wolcott-Rallison Syndrome

    Its characteristic clinical features are permanent neonatal or early infancy insulin-dependent diabetes and later onset skeletal dysplasia.[] Growth disturbance of the sternum and pectus deformities: imaging studies and clinical correlation.[] Wolcott-Rallison syndrome is a rare autosomal recessive condition characterized by early infancy onset diabetes mellitus and multiple epiphyseal dysplasia.[]

  • Sleep Disturbance

    313.89 Reactive Attachment Disorder of Infancy or Early Childhood 313.9 Disorder of Infancy, Childhood, or Adolescence NOS 314.00 Attention-Deficit/Hyperactivity Disorder[] Classes of fatigue and disturbed sleep severity were identified using latent growth mixture modeling.
.[] Type 312.89 Conduct Disorder, Unspecified Onset 312.9 Disruptive Behavior Disorder NOS 313.23 Selective Mutism 313.81 Oppositional Defiant Disorder 313.82 Identity Problem[]

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