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129 Possible Causes for Facial Hemihypertrophy

  • Bell's Palsy

    Bell's palsy represents a peripheral unilateral facial nerve paralysis, being an acute, idiopathic disorder, which can affect children and adolescents. Some therapeutic approaches have been proposed including facial exercises, biofeedback, photobiomodulation, electrotherapy, massage, and thermotherapy. The present[…][]

  • Congenital Hemihypertrophy

    hemihypertrophy and facial hemiatrophy are rare developmental anomalies.[] […] structural asymmetry / facial hemiatrophy / facial hemihypertrophy - Macrostomia / big mouth - Polydactyly of toes - Syndactyly of toes - Telangiectasiae of the skin - Upper[] Differential diagnosis Facial hemihypertrophy or hemimacrosomia or partial/unilateral gigantism characterized by marked unilateral overdevelopment of hard and soft tissues[]

  • Sturge-Weber Syndrome

    Sturge-Weber syndrome (SWS) is a rare and sporadic congenital neurocutaneous disorder, that is characterized by facial venous capillary malformation (port-wine birthmark), leptomeningeal venous malformation (angiomatosis), glaucoma, and neurologic problems. SWS can comorbid with other disorders in some patients,[…][]

  • Epidermal Nevus Syndrome

    All had ipsilateral epidermal nevi of the head, and several had ipsilateral facial hemihypertrophy.[] Pavone et al. (1991) identified a homogeneous variant of ENS with hemimegalencephaly, gyral malformation, mental retardation, seizures and facial hemihypertrophy.[] We report two cases with severe primary brain involvement, seizures, mental retardation, and facial hemihypertrophy.[]

  • Hemimegalencephaly

    A full-term female neonate presented with facial port-wine stain, cutaneous telangiectasia, left facial hemihypertrophy, and left hemimegalencephaly at birth and subsequently[] The simultaneous appearance of congenital infiltrating lipomatosis of the face that causes facial hemihypertrophy and ipsilateral hemimegalencephaly is extremely rare.[] hemihypertrophy and linear naevus.[]

  • Growth Failure

    […] children with extreme intrauterine growth retardation and characteristic facial features [4].[] In 1953, Silver et al reported two unrelated children with congenital hemihypertrophy, low birth weight, and short stature [7] and in 1954 Russell described five unrelated[]

  • Ectropion

    Neurofibromatosis, Prader-Willi syndrome, Rieger anomaly, and facial hemihypertrophy were found to occur concomitantly with CEU, suggesting the possibility of a neural crest[]

  • Facial Hemiatrophy

    hemihypertrophy and facial hemiatrophy are rare developmental anomalies.[] Progressive facial hemiatrophy]. Rev Stomatol Chir Maxillofac. 1983;84(6):313-21. Review. French.[] Facial hemihypertrophy and facial hemiatrophy: Report of 2 cases. J Indian Acad Oral Med Radiol [serial online] 2008 [cited 2019 May 14];20:57-9.[]

  • Nevus Sebaceous

    Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophy.[]

  • Proliferating Angioendotheliomatosis

    […] port-wine stain, macroglossia, omphalocele, visceral hyperplasia, hemihypertrophy, and hypoglycemia.[] […] port-wine, hemihypertrophy, macrodactyly, verrucous epidermal nevus, soft-tissue subcutaneous masses, and cerebriform overgrowth of the plantar surface.[] […] deep venous system malformations, superficial varicosities, bony and soft tissue hypertrophy 23 Klippel-Trenaunay Syndrome 24 Nevus Flammeus Beckwith-Wiedemann Syndrome; facial[]

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