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10 Possible Causes for Basal Cell Carcinoma, Cataract, Relative Macrocephaly in Childhood

  • Gorlin Syndrome

    […] syndrome (disorder) Naevoid basal cell carcinoma syndrome basal cell nevus syndrome Gorlin syndrome edit English nevoid basal cell carcinoma syndrome an autosomal dominant[wikidata.org] […] with NBCCS childhood medulloblastoma macrocephaly (occipital frontal circumference 97th centile) cleft lip/palate vertebral/rib anomalies preaxial or postaxial polydactyly[invitae.com] […] clinical features include: multiple basal cell carcinoma lesions on the skin palmar pits cysts within the mandible fused or bifid ribs calcification of the falx cerebri cataracts[gpnotebook.co.uk]

  • Neurofibromatosis Type 2

    Although this is usually of cosmetic significance only, melanoma and basal cell carcinoma have been reported in adults with NF1; however, the risk for developing these malignancies[pediatrics.aappublications.org] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[web.archive.org] We identified 3 types of NF2-associated lesions: juvenile posterior subcapsular cataracts, epiretinal membranes, and an intrascleral schwannoma.[ncbi.nlm.nih.gov]

  • Neurofibromatosis Type 1

    Gorlin Syndrome (nevoid basal cell carcinoma syndrome) Risk of developing cancerous and noncancerous tumors, most often basal cell carcinoma, less often meduloblastoma during[doi.org] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[web.archive.org] Figure 1: (A) Left juvenile posterior subcapsular cataract. Also note presence of ptosis on right side. (B) Café-au-lait spots and dermal fibroma.[medical-case-reports.imedpub.com]

  • Legius Syndrome

    Gorlin Syndrome (nevoid basal cell carcinoma syndrome) Risk of developing cancerous and noncancerous tumors, most often basal cell carcinoma, less often meduloblastoma during[scielo.br] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[ncbi.nlm.nih.gov] […] peripheral nerve schwannomas, meningiomas, ependymomas, and astrocytomas. 60–80% of patients with NF2 suffer from presenile posterior subcapsular lenticular opacities ( cataracts[dermnetnz.org]

  • Fitzsimmons-Guilbert Syndrome

    CELL NEVUS SYNDROME NEVOID BASAL CELL CARCINOMA (BCC) SYNDROME GORLIN-GOLTZ SYNDROME syndrome of autosomal dominant inheritance characterized by (1) multiple cutaneous basal[radiologykey.com] Relative macrocephaly is present during early childhood but head circumference is markedly low by adulthood. Psychomotor development is normal.[nectarmutation.org] She also has cataract.[entokey.com]

  • Zori-Stalker-Williams Syndrome

    Cell Carcinoma Bed Baths, Ayurveda Treatment For Bedwetting, Ayurveda Treatment For Benzodiazepine Abuse, Ayurveda Treatment For Bicycle Helmets Bicycle Safety, Ayurveda[ayurdoctor.com] […] nails syndrome is a rare multiple congenital anomalies syndrome characterized by relative macrocephaly, pectus excavatum, short stature, nail dysplasia, and motor developmental[orpha.net] Zonular cataract and nystagmus[?] Zori Stalker Williams syndrome[?] Zunich-Kaye syndrome[?] Zuska's Disease[?][encyclopedia.kids.net.au]

  • Nasopalpebral Lipoma - Coloboma - Telecanthus Syndrome

    Basal cell carcinoma B. Capillary hemangioma C. Conjunctiva amyloidosis 3. Medications A. Epinephrine B. Idoxuridine C. Phospholine iodide D. Pilocarpine E. Practolol F.[dentisty.org] ., 2017 Patient 4 Japanese case F M General characteristics Gender M Country of origin M F China M Germany Japan Clinical features Short stature Relative macrocephaly at birth[docksci.com] Syndromes and diseases associated with exophthalmos, ptosis, strabismus, nystagmus, glaucoma, cataracts, uveitis and optic atrophy are discussed in detail.[books.google.com]

  • Pseudohypoparathyroidism Type 1B

    : AGM3, 6 Integrin : LAD1 Glanzmann's thrombasthenia Junctional epidermolysis bullosa with pyloric atresia EDAR ( EDAR hypohidrotic ectodermal dysplasia ) PTCH1 ( Nevoid basal-cell[en.wikipedia.org] Many patients have relatively high birth weight and/or early-onset obesity that persists into childhood and later; relative macrocephaly and tall stature have also been observed[academic.oup.com] Symptoms usually begin in childhood due to low calcium levels and may include numbness, seizures, tetany, cataracts, and dental problems. [1] Excessive growth or weight has[rarediseases.info.nih.gov]

  • Stevenson Carey Syndrome

    cell carcinoma syndrome NF1 Microduplication Syndrome Nguyen Syndrome Nicolaides Baraitser Syndrome Nicolau Syndrome Nievergelt Syndrome Nijmegen breakage syndrome Nisch[rgd.mcw.edu] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[ncbi.nlm.nih.gov] Microcornea Syndrome Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome Cataracts, Ataxia, Short Stature, and Mental Retardation Cayler Cardiofacial Syndrome cerebellar[rgd.mcw.edu]

  • Opitz-Kaveggia Syndrome

    cell carcinoma syndrome, Basal Cell Nevus Syndrome, Gorlin syndrome 20301330 PTEN Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome (BRRS) PTEN related hamartoma syndrome[web.labmed.washington.edu] The key elements of the clinical phenotype are absolute or relative macrocephaly with a long narrow face; tall forehead; dolicocephalic head shape; an open mouth; small, simple[nature.com] […] dysmorphic facies–short nose with anteverted nares, ptosis of eyelids, micrognathia, poly- and/or syndactyly, genital disorders–cryptorchidism, hypospadias, endocrine defects, cataracts[medical-dictionary.thefreedictionary.com]

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