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  • ¿µ¹®
    ÇѱÛ
  • cartilage-hair hypoplasia
    ¿¬°ñÅÐÇü¼ºÀúÇÏÁõ
  • disc hypoplasia
    ½Ã(°¢)½Å°æÀ¯µÎÇü¼ºÀúÇÏ
  • focal dermal hypoplasia
    ±¹¼ÒÁøÇÇÇü¼ºÀúÇÏÁõ
  • genital hypoplasia
    »ý½Ä±â°üÇü¼ºÀúÇÏÁõ
  • hypoplasia
    Çü¼ºÀúÇÏÁõ, ÀúÇü¼º(Áõ)
  • mandibular hypoplasia
    ¾Æ·¡ÅλÀÇü¼ºÀúÇÏÁõ, ÇϾǰñ¹ßÀ°ºÎÀüÁõ
  • maxillary hypoplasia
    À§ÅλÀÇü¼ºÀúÇÏÁõ
  • macular hypoplasia
    Ȳ¹ÝÇü¼ºÀúÇÏÁõ
  • nasomaxillary hypoplasia
    ÄÚÀ§ÅÎÇü¼ºÀúÇÏÁõ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hypoplasia
    Çü¼ºÀúÇÏÁõ
  • Turner's syndrome
    ÅͳÊÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • cartilage-hair hypoplasia
    ¿¬°ñÅÐÇü¼ºÀúÇÏÁõ
  • disc hypoplasia
    ½Ã°¢À¯µÎÇü¼ºÀúÇÏ
  • focal dermal hypoplasia
    ±¹¼ÒÁøÇÇÇü¼ºÀúÇÏÁõ
  • genital hypoplasia
    »ý½Ä±â°üÇü¼ºÀúÇÏÁõ
  • hypoplasia
    Çü¼ºÀúÇÏÁõ
  • macular hypoplasia
    Ȳ¹ÝÇü¼ºÀúÇÏÁõ
  • mandibular hypoplasia
    ¾Æ·¡ÅλÀÇü¼ºÀúÇÏÁõ, ÇϾǰñ¹ßÀ°ºÎÀüÁõ
  • maxillary hypoplasia
    À§ÅλÀÇü¼ºÀúÇÏÁõ
  • nasomaxillary hypoplasia
    ÄÚÀ§ÅÎÇü¼ºÀúÇÏÁõ
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  • Goltzs syndrome => focal dermal hypoplasia
    ±¹¼Ò ÁøÇÇ Çü¼ººÎÀüÁõ
  • genital hypoplasia<³ª> h. genitalis
    ¼º±âÀúÇü¼º.
  • genital hypoplasia<³ª> h. genitalis
    ¼º±âÀúÇü¼º.
  • hereditary dentin hypoplasia
    À¯Àü¼º »ó¾ÆÁú Çü¼ººÎÀü(Áõ)(¡­ßÚä³òõû¡à÷ÝÕîï ñø).
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý³¶ Áú ÀúÇü¼ºÁõ.
  • renal hypoplasia
    ½Å¹ßÀ°ºÎÀü(ãìÛ¡ëÀÝÕîï).
  • renal hypoplasia
    ½Å¹ßÀ°ºÎÀü(ãìÛ¡ëÀÝÕîï)
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  • gonadal dysgenesis ; Turners syndrome
    ¼º¼±À̹߻ýÁõ(àõàÍì¶Û¡ßæñø) ; ÅͳÊÁõÈıº.
  • gonadal dysgenesis ; Turners syndrome
    ¼º¼±À̹߻ýÁõ(àõàÍì¶Û¡ßæñø) ; ÅͳÊÁõÈÄ__
  • male Turners syndrome
    ³²¼º ÅÍ³Ê ÁõÈıº
  • cartilage-hair hypoplasia
    ¿¬°ñ-¸ð¹ß Çü¼º ºÎÀüÁõ
  • congenital hypoplasia
    ¼±Ãµ¼º Çü¼ººÎÀü(Áõ)(¡­û¡à÷ÝÕîïñø).º´¸®¼±Ãµ¼º ÀúÇü¼º.
  • dental hypoplasia =oral h.
    Ä¡¾ÆÀúÇü¼º.
  • dermal hypoplasia
    ÁøÇÇÇü¼ººÎÀüÁõ
  • disc hypoplasia
    ½Ã½Å°æÀ¯µÎÇü¼ººÎÀü
  • enamel hypoplasia
    ¹ý³¶ÁúÀúÇü¼º.
  • genital hypoplasia<³ª> h. genitalis
    ¼º±âÀúÇü¼º.
  • genital hypoplasia<³ª> h. genitalis
    ¼º±âÀúÇü¼º.
  • hereditary dentin hypoplasia
    À¯Àü¼º »ó¾ÆÁú Çü¼ººÎÀü(Áõ)(¡­ßÚä³òõû¡à÷ÝÕîï ñø).
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý³¶ Áú ÀúÇü¼ºÁõ.
  • hypoplasia
    ÀúÇü¼º
  • hypoplasia
    ÀúÇü¼º, ¹ßÀ°ºÎÀü(Û¡ëÀÝÕîï), Çü¼ººÎÀü(û¡à÷ÝÕîï)
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  • gonadal dysgenesis; Turner's syndrome
    ¼º¼±À̹߻ýÁõ, ÅͳÊÁõÈıº
  • hypoplasia
    ÀúÇü¼º, ¹ßÀ°ºÎÀü, Çü¼ººÎÀü
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TOF   1) Tetralogy Of Fallot
    ? CIx of Corrective Op
  ...
PAGOD pulmonary hypoplasia-hypoplasia of pulmonary artery-agonadism-omphalocele/diaphragmatic defect-dextr...
TS Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str...
UT total unsharpness; Ullrich-Turner [syndrome]; Unna-Thost [syndrome]; untested; untreated; urinary tr...
UTS Ullrich-Turner syndrome; ulnar tunnel syndrome; ultimate tensile strength
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TS Turner Syndrome
UTS Ullrich-Turner Syndrome
AHC Adrenal hypoplasia congenita
CHH Cartilage hair hypoplasia
FDH Focal Dermal Hypoplasia
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  • Turner's syndrome
    ÅÍ³Ê ÁõÈıº
    ´Ü ½ÅÀå, ¹ÌºÐÈ­ »ý½Ä¼±, ±×¸®°í ÀÍ»ó°æ, ÀúÀ§¹ß°æ°è, ¿Ü¹Ý»ç, ½ÉÀå ±âÇüÀ¸¸£ Æ÷ÇÔÇÑ °¢Á¾ ±âÇüÀ» ÀÏÀ¸Å°´Â ¼º¼± ¹ßÀ° Àå¾Ö·Î X¿°»öü ÇÑ °³ÀÇ °áÇ̰ú ¸ðÀÚÀÌÅ© Çö»óµµ ³ªÅ¸³ªÁö¸¸, 2¹øÂ° X¿°»öüÀÇ °á¼ÕÀ» ³ªÅ¸³»´Â °ÍÀÌ ÀüÇüÀûÀÎ ÇüÅÂÀÌ´Ù. Ç¥ÇöÇüÀº ¿©¼ºÀ̸ç, ȯÀÚ´Â Ç×»ó ºÒÀÓÀÌ´Ù.
  • Turner's tooth
    ÅͳÊÄ¡
  • dermal hypoplasia
    ÁøÇÇ Çü¼º ºÎÀüÁõ
  • developmental hypoplasia
    ¹ß»ý Çü¼º ºÎÀü
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý¶ûÁú ÀúÇü¼ºÁõ
    Ä¡¾Æ ¹ý¶ûÁúÀÇ À¯ÀüÀû ºÒ¿ÏÀü Çü¼º ¶Ç´Â ¹ßÀ° ÀÌ»ó.
  • hypoplasia of adrenal gland
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  • hypoplasia of mandibular condyle
    ¾Ç°üÀý µ¹±â ¹ßÀ° ºÎÀü
  • maxillary hypoplasia
    ¾È¸é Á߾ӺΠÇü¼º ºÎÀü
  • renal hypoplasia
    ½Å ¹ßÀ° ºÎÀü
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parathyroids, hypoplasia of the thymusand Also known as the digeorge syndrome (dgs), this disorder is characterised by (1) low blood calcium levels (hypocalcaemia) due to underdevelopment (hypoplasia) of the parathyroid glands which control calcium; (2) underdevelopment (hypoplasia) of the thymus, an organ behind the breastbone in which lymphocytes mature and multiply; and (3) defects of the heart involving the outflow tracts from the heart. most cases of dgs are due to a microdeletion in chromosome band 22q11.2. A small number of cases have defects in other chromosomes, notably 10p13. Named after the american paediatric endocrinologist angelo digeorge. Another name for dgs is the third and fourth pharyngeal pouch syndrome.
(12 Dec 1998)
cartilage-hair hypoplasia An autosomal recessive form of dwarfism characterised by shortness of the extremities without skull defects, and with sparse, brittle hair of light colour. There is a peculiar, not adequately explained severity in the clinical course of varicella and herpes in such patients.
(05 Mar 2000)
renal hypoplasia An abnormally small kidney that is morphologically normal but has either a reduced number of nephrons or smaller nephrons.
(05 Mar 2000)
right ventricular hypoplasia A congenital or acquired condition in which there is thinning of the right ventricular myocardium.
Synonym: right ventricular hypoplasia.
(05 Mar 2000)
hypoplasia <embryology> The incomplete development or underdevelopment of an organ or tissue.
Origin: Gr. Plasis = formation
(18 Nov 1997)
hypoplasia of right ventricle Failure of development of the right ventricle resulting in its having little muscle and much connective tissue instead of the reverse.
(05 Mar 2000)
hypoplasia of the thymus and parathyroids Also known as the digeorge syndrome (dgs), this disorder is characterised by (1) low blood calcium levels (hypocalcaemia) due to underdevelopment (hypoplasia) of the parathyroid glands needed to control calcium; (2) underdevelopment (hypoplasia) of the thymus, an organ behind the breastbone in which lymphocytes mature and multiply; and (3) defects of the outflow tracts from the heart. most cases of dgs are due to a microdeletion in chromosome band 22q11.2. A small number of cases have defects in other chromosomes, notably 10p13. Named after the american paediatric endocrinologist angelo digeorge. Another name for dgs is the third and fourth pharyngeal pouch syndrome (since the faulty structures in dgs are embryologically derived from the third and fourth pharyngeal pouches).
(12 Dec 1998)
dental enamel hypoplasia <dentistry> A form of amelogenesis imperfecta characterised by incomplete formation of the dental enamel and transmitted as an x-linked or autosomal dominant trait. It is also associated with vitamin a, c, or d deficiency, infectious disease, prematurity, birth injury, rh incompatibility, trauma, or local infection. Small grooves, pits, and fissures are seen in mild cases, deep horizontal rows of pits in severe cases, or absence of enamel in extreme cases.
(12 Dec 1998)
optic nerve hypoplasia Congenitally small optic disk resulting from failure of development of retinal ganglion cells, with a reduced number of axons; visual impairment may be marked.
See: de Morsier's syndrome.
(05 Mar 2000)
thymic hypoplasia diGeorge syndrome
thymus and parathyroids, hypoplasia of See third and fourth pharyngeal pouch syndrome.
(12 Dec 1998)
enamel hypoplasia A developmental disturbance of teeth characterised by deficient or defective enamel matrix formation; may be hereditary, as in amelogenesis imperfecta, or acquired, as encountered in dental fluorosis, local infection, childhood fevers, and congenital syphilis.
(05 Mar 2000)
focal dermal hypoplasia A genetic skin disease characterised by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an x-linked dominant trait.
(12 Dec 1998)
Parsonage-Turner syndrome A neurological disorder, of unknown cause, characterised by the sudden onset of severe pain, usually about the shoulder and often beginning at night, soon followed by weakness and wasting of various forequarter muscles, particularly shoulder girdle muscles; both sporadic and familial in occurrence with the former much more common; often preceded by some antecedent event, such as an upper respiratory infection, hospitalization, vaccination, or non-specific trauma; usually attributed to a brachial plexus lesion, because the nerve fibres involed are most often derived from the upper trunk, but actually multiple proximal mononeuropathies.
Synonym: acute brachial radiculitis, brachial plexitis, brachial plexus neuropathy, Parsonage-Turner syndrome, shoulder-girdle syndrome.
(05 Mar 2000)
Grey Turner's sign <clinical sign> Local areas of discoloration about the umbilicus and in the region of the loins, in acute haemorrhagic pancreatitis and other causes of retroperitoneal haemorrhage.
(05 Mar 2000)
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