2014
DOI: 10.4103/0378-6323.129400
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Delleman syndrome or Haberland syndrome?

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Cited by 2 publications
(8 citation statements)
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“…15 Some of these conditions are Goldenhar (oculo-auriculo-vertebral) syndrome, Goltz–Gorlin syndrome (also named Goltz syndrome; this condition is characterised by focal dermal hypoplasia), Hallermann–Streiff syndrome (oculomandibulodyscephaly), encephalo-cranio-cutaneous lipomatosis (ECCL or Haberland or Fishman syndrome), Aicardi syndrome, periventricular nodular heterotopia–polymicrogyria syndrome. 3,6,1416 The peri-ocular location of the skin tags (rather than preauricular) and the lack of vertebral anomalies make Gold-enhar syndrome unlikely in our patient. 3,4,9 The characteristic intracranial lipomatosis of ECCL as well as nevus psiloliparus was absent in our patient thus ruling out this diagnosis.…”
Section: Discussionmentioning
confidence: 82%
“…15 Some of these conditions are Goldenhar (oculo-auriculo-vertebral) syndrome, Goltz–Gorlin syndrome (also named Goltz syndrome; this condition is characterised by focal dermal hypoplasia), Hallermann–Streiff syndrome (oculomandibulodyscephaly), encephalo-cranio-cutaneous lipomatosis (ECCL or Haberland or Fishman syndrome), Aicardi syndrome, periventricular nodular heterotopia–polymicrogyria syndrome. 3,6,1416 The peri-ocular location of the skin tags (rather than preauricular) and the lack of vertebral anomalies make Gold-enhar syndrome unlikely in our patient. 3,4,9 The characteristic intracranial lipomatosis of ECCL as well as nevus psiloliparus was absent in our patient thus ruling out this diagnosis.…”
Section: Discussionmentioning
confidence: 82%
“…Las anomalías neurológicas incluyen convulsiones, trastornos del desarrollo psicomotor (polimicrogiria, colpocefalia, malformaciones del sistema ventricular, hidrocefalia, cavidades quísticas en los hemisferios cerebrales o cerebelo y agenesia del cuerpo calloso). Estas malformaciones de línea media y mesencéfalo son patognomónicas (9,12) . Entre las anomalías oculares asociadas se incluyen anoftalmia / microftalmia (unilateral o bilateral) con o sin quistes orbitales y colobomas del iris (1) .…”
Section: Discussionunclassified
“…Entre las anomalías oculares asociadas se incluyen anoftalmia / microftalmia (unilateral o bilateral) con o sin quistes orbitales y colobomas del iris (1) . Los quistes orbitales han sido descritos como quistes dermoides, encefalocele orbital, quistes con estructura de hamartomas neuroepiteliales, pared quística rodeada por neuroepitelio y tejidos gliales o tejidos epiteliales vestigiales de la retina (11,12) . Las alteraciones cutáneas incluyen áreas de aplasia o hipoplasia focal, alopecia y formación de los apéndices cutáneos perioculares característicos.…”
Section: Discussionunclassified
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