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1,168 Possible Causes for Possibly Scoliosis, Tall Stature

Did you mean: Possibly, Scoliosis, Tall Stature

  • Marfan Syndrome

    Vision problems should be treated when possible. Monitor for scoliosis, especially during the teenage years.[] It is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and sublaxation of the lens A hereditary disorder[] Treatment Vision problems should be treated when possible. Monitor for scoliosis, especially during the teenage years.[]

  • Straight Back Syndrome

    Today surgeons are often able to correct scoliosis while keeping as much as possible of the normal curves of the spine.[] […] of normal thoracic kyphosis, which AP chest diameter, prominence of pulmonary artery and right hilum, displacing heart to left, simulating cardiomegaly Associations ASD, scoliosis[] . • There may be an associated scoliosis • Narrow AP diameter of the thorax – Measured on lateral chest from the anterior border of T8 to the posterior border of the sternum[]

  • Klinefelter Syndrome

    Osteoporosis may lead to vertebral collapse and even scoliosis.[] These patients usually present with tall stature. We report a case of KS with short stature due to growth hormone deficiency.[] Physical examination revealed tall stature, thin built, small testes size, and absence of beard and pubic hairs.[]

  • Sotos Syndrome

    Other possible symptoms and signs can include: behavioral disturbances, intellectual disability, scoliosis, seizures, heart defects, kidney defects, weak muscle tone, stuttering[] Constitutional tall stature Tall stature in childhood usually presents less initial concern than short stature because, at least in early childhood, being tall can be advantageous[] A percentage of these patients develop progressive scoliosis early in life.[]

  • Gigantism

    Voice is hoarse and affected individuals have a plump, stocky body with pectus excavatum, thoracic scoliosis, hepatosplenomegaly, umbilical and/or inguinal hernias, broad[] This boy appears likely to have neurofibromatosis type 1 (NF1) which raises the question of subtle GH excess in NF1 patients with tall stature.[] Most common causes of tall stature/growth acceleration Normal variant genetic tall stature Endocrine abnormalities Precocious puberty Hyperthyroidism Gigantism Exogenous obesity[]

  • Marshall-Smith Syndrome

    […] laryngomalacia, glossoptosis, choanal stenoses, bilateral peripheral hearing defect, ventriculomegaly, congenital heart disease (atrial septal defect), chronic pulmonary disease, and scoliosis[] stature Increased body height 0000098 Thick eyebrow Bushy eyebrows Dense eyebrow Heavy eyebrows Prominent eyebrows Thick eyebrows [ more ] 0000574 Umbilical hernia 0001537[] […] nuclear factor I/X (NFIX) deletions or nonsense mutation in three sporadic cases of a Sotos-like overgrowth syndrome with advanced bone age, macrocephaly, developmental delay, scoliosis[]

  • Kyphoscoliosis

    The main aim of physical therapy is to make the spinal tissues stronger in order to help correct the curvature as much as possible.[] stature Cutis marmorata Obsessive-compulsive behavior Ectopia lentis Brittle hair Schizophrenia Pancreatitis Depressivity Tall stature Dental crowding Myocardial infarction[] […] idiopathic thoracic scoliosis Adolescent idiopathic thoracolumbar scoliosis Idiopathic adolescent scoliosis Idiopathic juvenile scoliosis Idiopathic scoliosis Juvenile idiopathic[]

  • Acromegaly

    He died as a result of pulmonary compromise secondary to advanced scoliosis. Fig. 1.[] Convert to ICD-10-CM : 253.0 converts approximately to: 2015/16 ICD-10-CM E22.0 Acromegaly and pituitary gigantism Approximate Synonyms Acromegaly Constitutional tall stature[] stature 2016 2017 2018 2019 Billable/Specific Code Applicable To Constitutional gigantism E34.4 ) constitutional tall stature ( ICD-10-CM Diagnosis Code E34.4 Constitutional[]

  • Homocystinuria

    The two diseases should be differentiated because of the thrombotic risk in homocystinuria, and also because in this disease there is a possibility of treating the biochemical[] Autosomal recessive disease caused by cystathionine synthase deficiency Patients normal at birth, then begin to develop developmental delays History / PE : Marfan features (tall[] Presentation Skeletal features: Marfanoid habitus with normal to tall stature (occasionally failure to thrive in infancy), fine, brittle hair, hypopigmentation, high arched[]

  • Klinefelter's Syndrome with XY/XXY Mosaic

    Occasional abnormalities may include cryptorchidism, hypospadias, ataxia, scoliosis during adolescence, and diabetes mellitus in adulthood.[] stature with eunuchoid features, and psychosocial morbidity. 1 3 How common is Klinefelter’s syndrome?[] […] increased risks for cognitive disabilities, disruptive behaviors, dysmorphic features, neurological abnormalities including seizures, and skeletal abnormalities such as scoliosis[]

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