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237 Possible Causes for Laurence Moon Syndrome, Midline Defects

  • Hypogonadism

    Other manifestations include microphallus, cryptorchidism, midline defects, and unilateral kidney agenesis.[msdmanuals.com] CHH is also a feature of several syndromes including the Prader-Willi, Bardet-Biedl, Laurence-Moon and CHARGE syndromes (see these terms).[orpha.net] syndrome, Sheehan syndrome, Kallmann's disease, Laurence-Moon-Biedl disease, Lowe syndrome, Prader-Willi syndrome. hy·po·go·nad·ism ( hī'pō-gō'nad-izm ) Inadequate gonadal[medical-dictionary.thefreedictionary.com]

  • Mental Retardation

    Further studies will explore the specific mechanisms whereby PHF8 alterations lead to mental retardation and midline defects.[ncbi.nlm.nih.gov] The association of PHF8 with mental retardation and midline defects highlights the importance of this process, specifically during brain development and midline formation.[doi.org]

  • Hypodontia

    Cdon mutation and fetal ethanol exposure synergize to produce midline signaling defects and holoprosencephaly spectrum disorders in mice. PLoS Genet. 8(10): e1002999.[doi.org] Els-Marie Andersson, Stefan Axelsson, Lars-Fredrik Gjølstad and Kari Storhaug, Taurodontism: A minor diagnostic criterion in Laurence-Moon/Bardet-Biedl syndromes, Acta Odontologica[doi.org]

  • Kallmann Syndrome

    Abstract Kallmann syndrome (isolated hypogonadotropic hypogonadism) is associated with a number of midline defects, especially anosmia.[doi.org] […] other than HGH Isolated follitropin deficiency Isolated gonadotropin deficiency Isolated lutropin deficiency Isolated prolactin deficiency Isolated thyroliberin deficiency Laurence-Moon[icd9data.com] MR images of midline defects in Kallmann syndrome were rarely seen in the literature.[jofem.org]

  • Hypogonadotropic Hypogonadism 4

    Occasionally the diagnosis is made earlier due to investigation of other associated anomalies, including: midline defects cleft lip and palate renal agenesis sensorineural[radiopaedia.org] […] other than HGH Isolated follitropin deficiency Isolated gonadotropin deficiency Isolated lutropin deficiency Isolated prolactin deficiency Isolated thyroliberin deficiency Laurence-Moon[icd9data.com] It is characterized by congenital hypogonadotropic hypogonadism and anosmia, possibly with additional midline defects.[icd10data.com]

  • Hypogonadotropic Hypogonadism 3

    Occasionally the diagnosis is made earlier due to investigation of other associated anomalies, including: midline defects cleft lip and palate renal agenesis sensorineural[radiopaedia.org] Laurence-Moon syndrome is characterized by obesity, intellectual disability, retinitis pigmentosa, and polydactyly.[msdmanuals.com] […] producing GRH–gonadotropin-releasing hormone; FSH and LH impairs sperm and androgen production Clinical Delayed puberty, micropenis, eunuchoid features, cryptorchidism, midline[medical-dictionary.thefreedictionary.com]

  • Exotropia

    Patients with craniofacial syndromes, ocular albinism, midline defects, and cerebral palsy may present with congenital exotropia.[emedicine.com] , Apert syndrome, Noonan syndrome, Prader-Willi syndrome, trisomy 18, congenital rubella, incontinentia pigmenti, cerebral palsy, Laurence-Moon-Biedl syndrome, pseudohyperparathyroidism[medical-dictionary.thefreedictionary.com] Congenital exotropia: Congenital exotropia is rare and present at birth and may be associated with neurological abnormalities like cerebral palsy, midline defects or craniofacial[aimu.us]

  • Luteinizing Hormone Deficiency

    There was no anosmia, midline defects or gynaecomastia. He had scanty pubic hair which came only after testosterone injection (Tanner stage 2) but no axillary hair.[endocrine-abstracts.org] […] other than HGH Isolated follitropin deficiency Isolated gonadotropin deficiency Isolated lutropin deficiency Isolated prolactin deficiency Isolated thyroliberin deficiency Laurence-Moon[icd9data.com] It is characterized by congenital hypogonadotropic hypogonadism and anosmia, possibly with additional midline defects.[icd10data.com]

  • Melhem-Fahl Syndrome

    […] cleft of lower lip Midline defects autosomal type Midline defects recessive type Midline developmental field defects Midline field defects Midline lethal granuloma Mietens[bioreference.net] syndrome LaurenceMoon–Bardet–Biedl syndrome Laurin–Sandrow syndrome Laxova–Brown–Hogan syndrome Lb–Lc LBWC - amniotic bands LBWD syndrome LCHAD deficiency Le Lea–Leh • Lei–Ler[sosu.us] […] type Midline defects recessive type Midline developmental field defects Mievis Verellen Dumoulin syndrome Milner Khallouf Gibson syndrome Minkowski-Chauffard disease Minoxidil[mindmappedia.com]

  • Anterior Pituitary Hypofunction

    It is characterized by congenital hypogonadotropic hypogonadism and anosmia, possibly with additional midline defects.[icd10data.com] […] other than HGH Isolated follitropin deficiency Isolated gonadotropin deficiency Isolated lutropin deficiency Isolated prolactin deficiency Isolated thyroliberin deficiency Laurence-Moon[icd9data.com] […] growth hormone Isolated follitropin deficiency Isolated gonadotropin deficiency Isolated lutropin deficiency Isolated prolactin deficiency Isolated thyroliberin deficiency Laurence-Moon[healthprovidersdata.com]

Further symptoms