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  • ...ated with [[Weill-Marchesani syndrome]], [[Marfan syndrome]], and [[Alport syndrome]]. It can also occur as a result of spontaneous mutations. * [[Weill-Marchesani syndrome]]
    1 KB (164 words) - 03:50, 22 February 2024
  • * '''[[Classical Ehlers-Danlos syndrome]]''' * '''[[Dermatosparaxis Ehlers-Danlos syndrome]]'''
    1 KB (135 words) - 13:24, 23 June 2020
  • | name = WeillMarchesani syndrome ...pherophakia-brachymorphia syndrome, congenital mesodermal dystrophy, GEMSS syndrome
    4 KB (461 words) - 02:46, 7 April 2021
  • ...related FBN1 and FBN2 genes cause [[Marfan syndrome]], [[Weill-Marchesani syndrome]], and other connective tissue disorders. Further research is needed to det * [[Marfan syndrome]]
    1 KB (201 words) - 23:29, 25 February 2024
  • ...sociated with several medical conditions. These include [[Weill-Marchesani syndrome]], a rare genetic disorder characterized by short stature, brachydactyly, j * [[Weill-Marchesani syndrome]]
    1 KB (192 words) - 21:25, 9 March 2024
  • ...the FBN1 gene are associated with [[Marfan syndrome]], [[Weill-Marchesani syndrome]], and [[acromicric dysplasia]]. These are all heritable disorders affectin * [[Marfan syndrome]]
    2 KB (197 words) - 03:01, 22 February 2024
  • ...a disorder affecting the body's connective tissue, and [[Weill-Marchesani syndrome]], a rare disorder that affects the body's connective tissue and causes sho * [[Marfan syndrome]]
    2 KB (196 words) - 22:22, 3 March 2024
  • ...]], [[Ehlers-Danlos syndrome]], [[Homocystinuria]], and [[Weill-Marchesani syndrome]]. In some cases, it can also be a congenital condition, meaning it is pres * [[Marfan syndrome]]
    2 KB (255 words) - 04:08, 4 March 2024
  • ...eye, or certain diseases such as [[Marfan syndrome]] or [[Weill-Marchesani syndrome]]. * [[Marfan syndrome]]
    2 KB (278 words) - 13:47, 25 February 2024
  • ...ghr.nlm.nih.gov/condition/ophthalmo-acromelic-syndrome Ophthalmo-acromelic syndrome]''' * '''[https://ghr.nlm.nih.gov/condition/waardenburg-syndrome Waardenburg syndrome]'''
    10 KB (1,412 words) - 21:01, 18 March 2024
  • * '''[[W syndrome]]''' * '''[[Waaler-Aarskog syndrome]]'''
    9 KB (1,233 words) - 03:39, 10 April 2022
  • * '''[[WAGR Syndrome]]''' * '''[[Waardenburg Syndrome]]'''
    7 KB (990 words) - 03:46, 10 March 2024
  • * '''[https://ghr.nlm.nih.gov/condition/baller-gerold-syndrome Baller-Gerold syndrome]''' * '''[[Ballinger-Wallace syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/maternally-inherited-diabet
    35 KB (4,381 words) - 20:55, 18 March 2024
  • ...haly-capillary-malformation-syndrome Megalencephaly-capillary malformation syndrome]''' ...ghr.nlm.nih.gov/condition/lenz-microphthalmia-syndrome Lenz microphthalmia syndrome]'''
    93 KB (11,515 words) - 20:58, 18 March 2024
  • * '''[[12q14 microdeletion syndrome]]''' * '''[[2q37 deletion syndrome]]'''
    28 KB (3,384 words) - 06:49, 23 June 2020
  • * '''[[12q14 microdeletion syndrome]]''' * '''[[2q37 deletion syndrome]]'''
    28 KB (3,461 words) - 22:48, 18 September 2019
  • * '''[[Ablepharon macrostomia syndrome]]''' * '''[[ADULT syndrome]]'''
    32 KB (4,068 words) - 15:17, 21 June 2020
  • ...s://ghr.nlm.nih.gov/condition/caudal-regression-syndrome Caudal regression syndrome]''' ...s://ghr.nlm.nih.gov/condition/caudal-regression-syndrome Caudal regression syndrome]'''
    72 KB (9,054 words) - 21:00, 18 March 2024
  • ...'''[https://ghr.nlm.nih.gov/condition/bohring-opitz-syndrome Bohring-Opitz syndrome]''' * '''[[CACH syndrome]]''' see '''[https://ghr.nlm.nih.gov/condition/leukoencephalopathy-with-va
    114 KB (14,485 words) - 20:56, 18 March 2024
  • ...ly in disease state or condition. For example, children born with [[Down's syndrome]] have learning difficulties, mental retardation, a characteristic facial a * '''[[A R syndrome]]'''
    129 KB (17,733 words) - 17:47, 19 March 2024

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