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170 Possible Causes for Funnel Chest, Possibly Scoliosis, Tall Stature

Did you mean: Funnel Chest, Possibly, Scoliosis, Tall Stature

  • Marfan Syndrome

    Pectus excavatum is a condition in which the breast bone (sternum) appears sunken and the chest concave. It is sometimes called funnel chest.[] 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[]

  • 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[] Pectus excavatum is a condition in which the breast bone (sternum) appears sunken and the chest concave. It is sometimes called funnel chest.[] Autosomal recessive disease caused by cystathionine synthase deficiency Patients normal at birth, then begin to develop developmental delays History / PE : Marfan features (tall[]

  • Marshall-Smith Syndrome

    […] laryngomalacia, glossoptosis, choanal stenoses, bilateral peripheral hearing defect, ventriculomegaly, congenital heart disease (atrial septal defect), chronic pulmonary disease, and scoliosis[] chest 0000767 Prominence of the premaxilla Anterior position of the premaxilla Anterior position of the primary palate bone Prominence of the primary palate bone [ more ][] […] 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[]

  • Cleidocranial Dysplasia

    […] the spaces between the bones of the skull Underdeveloped cheekbones and prominent brow bone Wide nasal bridge due to increased space between the eyes High arched palate or possible[] CADASIL NGS panel HTRA1, NOTCH3 Del Dup NGS Caffey disease COL1A1 Del Dup NGS Campomelic dysplasia SOX9 Del Dup NGS Camptodactyly, tall stature, and hearing loss syndrome[] The possibility of syringomyelia should be considered in patients with cleidocranial dysostosis, especially those with neurologic symptoms, scoliosis not responding to conservative[]

  • Klinefelter Syndrome

    chest: one case Small forehead: one case.[] 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.[]

  • Distal Symphalangism

    chest) Other skull abnormality Movement disorder - dystonia/chorea/tremor/spasm Long philtrum Bell-shaped chest Hyperostotic/wide clavicle EEG abnormality Deeply grooved[] Five members of a kindred with brachydactyly and distal symphalangism, normal stature, pes cavus, and scoliosis were ascertained.[] stature 33 HP:0000098 21 short 1st metacarpal 33 HP:0010034 22 broad foot 33 HP:0001769 23 single transverse palmar crease 33 HP:0000954 24 camptodactyly 60 Occasional (29[]

  • Klinefelter's Syndrome with XY/XXY Mosaic

    chest: one case Small forehead: one case.[] 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?[]

  • 48,XXXY Syndrome

    chest: one case Small forehead: one case.[] Pulmonary embolism;HP:0002205 Recurrent respiratory infections;HP:0002564 Malformation of the heart and great vessels;HP:0002648 Abnormality of calvarial morphology;HP:0002650 Scoliosis[] While often compared with 47,XXY/Klinefelter syndrome because of shared features including tall stature and hypergonadotropic hypogonadism, 48,XXYY, 48,XXXY and 49,XXXXY syndromes[]

  • 48,XXYY Syndrome

    chest: one case Small forehead: one case.[] , leg ulcers, elbow abnormalities, curvature of the little finger (known as ‘clindactyly’), stretchy joints (known as ‘hypermobility’), curvature of the spine (known as ‘scoliosis[] It has similarities to 47, XXY Klinefelter's syndrome, with tall stature, micro-orchidism, hypergonadotropic hypogonadism and infertility in males.[]

  • Disproportionate Short Stature - Ptosis - Valvular Heart Lesions

    The neck is short, and the children may have bone deformities affecting the spine (kyphosis/scoliosis), or the chest (funnel chest or shield chest).[] Other Possible Symptoms Curved spine, called scoliosis Ear infections Early puberty Farsightedness Hernia High levels of calcium in the blood Hoarse voice Joint and bone problems[] Search terms included short stature, tall stature, and growth hormone.[]

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