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382 Possible Causes for Congenital Clubfoot, Mental Retardation

  • Alpha-Mannosidosis

    All patients showed mental retardation and hearing loss from early childhood.[ncbi.nlm.nih.gov] Clinical symptoms include coarse facial features, skeletal involvement (dysostosis multiplex), hearing disabilities, mental retardation and hepatosplenomegaly.[ncbi.nlm.nih.gov] Human alpha-mannosidosis is a lysosomal storage disorder characterized by mental retardation, dysostosis multiplex, and hepatosplenomegaly.[ncbi.nlm.nih.gov]

  • Patau Syndrome

    The initial clinical examination detected polydactyly in the left hand, congenital clubfoot and convex soles, ocular hypertelorism, a low nasal bridge, numerous hemangiomas[ncbi.nlm.nih.gov] Survivors suffer from severe mental retardation and health problems all their lives.[symptoma.com] The initial clinical examination detected polydactyly in the left hand, congenital clubfoot and convex foot soles.[funpecrp.com.br]

  • Klinefelter Syndrome

    Congenital malformations including congenital heart defects, radioulnar synostosis, cleft palate (submucosal or occult), hip dysplasia, kidney dysplasia, clubfoot and inguinal[ncbi.nlm.nih.gov] This is the first description of KS, mosaicism (46,XY/47,XXY), associated with AN and mental retardation.[ncbi.nlm.nih.gov] Author information 1 Oasi Institute (IRCCS) for Research on Mental Retardation and Brain Aging, Troina, Italy. micezia@tiscali.it, msalemi@oasi.en.it. 2 Section of Endocrinology[ncbi.nlm.nih.gov]

  • Congenital Vertical Talus

    […] asymmetric talipes Congenital clubfoot NOS Congenital talipes NOS Congenital tarsal coalition Hammer toe, congenital Q66.9 Congenital deformity of feet, unspecified Abbreviations[icd10coded.com] retardation Rigid deformity at birth PowerPoint Presentation: Group II – neurogenic type Accompanied by muscle imbalance Associated with myelomeningocele or neurofibromatosis[authorstream.com] retardation [ 6 – 10 ].[bmcresnotes.biomedcentral.com]

  • Microcephaly

    , including severe microcephaly, intracranial calcifications, and other brain anomalies, sometimes accompanied by eye findings, redundant scalp skin, arthrogryposis, and clubfoot[doi.org] No clear consensus has been established regarding the management of oral cancer in patients with mental retardation.[ncbi.nlm.nih.gov] Hyperphosphatasia with mental retardation syndrome-3 is an autosomal recessive disorder usually characterized by severe mental retardation.[ncbi.nlm.nih.gov]

  • Sjogren-Larsson Syndrome

    先天性異常 congenital abnormality 先天性副腎過形成 congenital adrenal hyperplasia 先天性腎尿路奇形 congenital anomalies of the kidney and urinary tract 先天性無トランスフェリン血症 Congenital atransferrinemia[lsd-project.jp] When ichthyosis is associated with spasticity and mental retardation, one should consider SLS.[ncbi.nlm.nih.gov] His quadriplegia was managed by aggressive physiotherapy and mental retardation by stimulation techniques.[ncbi.nlm.nih.gov]

  • Pierre Robin Syndrome

    clubfoot, and short fingers and toes.[molecularcytogenetics.biomedcentral.com] retardation, severe seizures, skeletal (limb) abnormalities, small head (microcephaly), small lower jaw (micrognathia) and undescended testicles (cryptorchidism).[doi.org] Keyword: Pierre Robin syndrome, Sleep apnea syndrome, Mental retardation pp.1079-1083 発行日 1995年10月15日 Published Date 1995/10/15 DOI Copyright 1995, Igaku-Shoin Ltd.[webview.isho.jp]

  • Scott Bryant Graham Syndrome

    […] with unilateral Aerobic actinomyces infection Craniotubular syndrome Urban Schosser Spohn syndrome clubfoot unsegmented bar Hereditary multiple diaphyseal congenital with[yumpu.com] Title Other Names: Craniodigital syndrome with mental retardation; Craniodigital syndrome-mental retardation, Scott type; Scott craniodigital syndrome with mental retardation[rarediseases.info.nih.gov] […] epiphyseal dysplasia Advanced sleep phase syndrome syndrome Hereditary mucoepithelial dysplasia MATN3 related Scoliosis as part of NF Multiple epiphyseal dysplasia with Scoliosis congenital[yumpu.com]

  • Wolcott-Rallison Syndrome

    Certain malformations such as clubfoot or cleft palate can be present at birth (congenital). rMED is caused by mutations in the SLC26A2 gene.[rarediseases.org] Wolcott-Rallison syndrome has been reported to be associated with early-onset diabetes, epiphyseal dysplasia, hepatic and renal dysfunction, mental retardation, severe growth[ncbi.nlm.nih.gov] In addition to neonatal diabetes mellitus and epiphyseal dysplasia, this child had mental retardation and recurrent episodes of self-limiting hepatic failure.[ncbi.nlm.nih.gov]

  • Trisomy 18

    . view 75 KB version Here is a lateral cleft in a child with multiple congenital anomalies.[medgen.genetics.utah.edu] Various congenital malformations, mental retardation, and high rate of infant mortality in the first year of life are characteristic features of trisomy 18.[ncbi.nlm.nih.gov] It causes severe congenital abnormalities and mental retardation although phenotypic features, clinical manifestations and prognosis vary occasionally.[ncbi.nlm.nih.gov]

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