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100 Possible Causes for Macrocephaly (26, )

  • Familial Adenomatous Polyposis

    Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics. 1960. 26:293-300. Bannayan GA.[emedicine.medscape.com]

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  • Basal Cell Carcinoma

    50 Congenital Hypertelorism 42 Congenital Osseous lucencies in the hands 30 Congenital Frontal bossing 27 Congenital Bifid ribs 26 Congenital Calcification of tentorium cerebelli[cancer.gov] Palmar/plantar pits 87 Usually by age 10 y Keratogenic jaw cysts 74 Usually by age 20 y Bridged sella 68 Congenital Calcification of falx cerebri 65 Usually by age 40 y Macrocephaly[cancer.gov]

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  • Breast Hamartoma

    Am J Med Genet 2001; 105 : 521–524. 26. Reardon W, Zhou XP, Eng C.[nature.com] A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association. J Med Genet 2001; 38 : 820–823. 27.[nature.com]

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  • Central Precocious Puberty

    […] particular, 25 children were diagnosed with OPG after brain and orbit MRI was performed because of the presence of signs and/or symptoms suggestive of OPG; the remaining 26[mdpi.com] […] did not show symptoms related to OPG at the diagnosis and underwent brain imaging because of other clinical indications (including macrocephaly, developmental delay, headache[mdpi.com]

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  • Juvenile Polyp

    Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics . 1960. 26:293-300. Bannayan GA.[emedicine.medscape.com] Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics. 1960. 26:293-300. Bannayan GA.[emedicine.medscape.com]

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  • Hereditary Mixed Polyposis Syndrome

    Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics . 1960. 26:293-300. Bannayan GA.[emedicine.medscape.com]

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  • Juvenile Polyposis Syndrome

    Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics. 1960. 26:293-300. Bannayan GA.[emedicine.medscape.com]

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  • Writer's Cramp

    […] disorder characterized by macrocephaly, seizures, progressive mental retardation, pyramidal signs, ataxia and tremor.[clinicalmovementdisorders.biomedcentral.com] .; licensee BioMed Central Ltd. 2014 Received: 3 July 2014 Accepted: 26 September 2014 Published: 11 December 2014 Abstract L-2-hydroxyglutaric aciduria (L2HGA) is a neurometabolic[clinicalmovementdisorders.biomedcentral.com]

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  • Autosomal Dominant Prognathism

    […] cataracts,beaked nose, micrognathia, anteriorly placed mandibular condyles,natal teeth ; oligodontia; short stature www.indiandentalacademy.com 25. www.indiandentalacademy.com 26[slideshare.net] Striking features – Macrocephaly ; frontal and biparietal bossing;dystopia canthorum or ocular hypertelorism; mild mandibular prognathism;jaw cysts ; multiple basal cell carcinomas[slideshare.net]

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  • Autosomal-Recessive Robinow Syndrome

    Autosomal recessive Robinow syndrome (RRS) is a severe skeletal dysplasia with short stature, generalized limb shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. The gene encoding receptor orphan receptor tyrosine kinase 2 (ROR2) is located on chromosome 9q22 and[…][ncbi.nlm.nih.gov]

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