Create issue ticket

6,808 Possible Causes for Disharmonic Maturation of Phalanges and Carpal Bones, Mostly Sporadic, Neurological Disorder

  • Sotos Syndrome

    Abstract Sotos syndrome, described in 1964, was characterized by overgrowth, a distinctive craniofacial configuration, and a non-progressive neurological disorder with mental[ncbi.nlm.nih.gov] Citing Literature Number of times cited according to CrossRef: 3 Chloe Lane and Megan Freeth, Sotos syndrome, Chromatin Signaling and Neurological Disorders, 10.1016/B978-[doi.org] This answer is based on source information from the National Institute of Neurological Disorders and Stroke.[sharecare.com]

  • Poland Syndrome

    There have been described in the medical literature associations of Poland syndrome with Moebius syndrome (neurological disorder which is characterized by facial paralysis[medichub.ro] External links [ edit ] Möbius syndrome at Curlie Möbius syndrome at the National Institute of Neurological Disorders and Stroke[en.wikipedia.org] Möbius syndrome is an extremely rare congenital neurological disorder which is characterized by facial paralysis and the inability to move the eyes from side to side.[en.wikipedia.org]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Facial Hemiatrophy

    The NINDS supports research on neurological disorders such as Parry-Romberg syndrome with the goal of finding ways to prevent, treat, and cure them.[faces-cranio.org] Disorders and Stroke.[medicinenet.com] […] material is provided for information purposes only and does not necessarily represent endorsement by or an official position of the National Institute of Neurological Disorders[faces-cranio.org]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Encephalitis

    Louis encephalitis virus Mostly in urban areas of the central and southeastern US but also in western states — Occurs in periodic urban epidemics; otherwise sporadic and rare[merckmanuals.com] Both disorders are usually triggered by viruses. Symptoms include fever, headache, and altered mental status, often accompanied by seizures or focal neurologic deficits.[merckmanuals.com] Permanent neurologic deficits are common among patients who survive severe infection.[merckmanuals.com]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Alpers Syndrome

    EYE FINDING MODE OF INHERITANCE KNOWN GENES OR CHROMOSOMAL ABNORMALITY INVOLVED MIM SYMBOL & NUMBER REFERENCE VACTERL ASSOCIATION WITH HYDROCEPHALUS Downward gaze of eyes Mostly[eyewiki.aao.org] Get Update Overview Alpers syndrome is a progressive neurologic disorder that begins during childhood and is complicated in many instances by serious liver disease.[diseaseinfosearch.org] disorder that begins during childhood and is complicated in many instances by serious liver disease.[rarediseases.info.nih.gov]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Hereditary Hyperekplexia

    However, the hyperekplexia plus syndrome is extremely rare and mostly sporadic and occasionally genetic studies need to be done attention to other system-related complications[pediatricneurosciences.com] Abstract We investigated the molecular basis of hyperekplexia (STHE), an inherited neurological disorder characterised by neonatal hypertonia and an exaggerated startle response[ncbi.nlm.nih.gov] Hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses. Within the disorder two clinical forms can be distinguished.[ncbi.nlm.nih.gov]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Russell-Silver Syndrome

    Cases of Russell-Silver syndrome are mostly sporadic, that is, the disorder may appear in people with no known history of the disease in the family.[symptoma.com] […] type Congenital malformation syndromes with metabolic disturbances Congenital muscular hypertrophy-cerebral syndrome Congenital sequelae of disorders Congenital viral hepatitis[icd9data.com] […] arachnodactyly Congenital hemihypertrophy Congenital iodine deficiency syndrome Congenital iodine deficiency syndrome - mixed type Congenital iodine deficiency syndrome - neurological[icd9data.com]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Phenylketonuria

    Phenylalanine (Phe) deficiency and its clinical manifestations have been previously described mostly as sporadic case reports dating back to the 1960's and 1970's.[ncbi.nlm.nih.gov] Phenylketonuria cannot be fully treated however using a low phenylalanine diet can normalize phenylalanine concentrations and can prevent neurological disorders to some extent[web.archive.org] Treated people may have no detectable physical, neurological, or developmental problems at all. PKU is an autosomal recessive metabolic genetic disorder.[en.wikipedia.org]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Polyneuropathy

    Cramping pain occurred sporadically in my arms and legs, especially after any effort.[bruno-groening.org] Charcot-Marie-Tooth disease, also known as hereditary motor and sensory neuropathy, is one of the most common inherited neurological disorders.[ninds.nih.gov] Definition Treatment Prognosis Clinical Trials Organizations Publications Definition Chronic inflammatory demyelinating polyneuropathy (CIDP) is a neurological disorder characterized[ninds.nih.gov]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones
  • Opsoclonus-Myoclonus Syndrome

    The disorder is sporadic and occurs in people with no family history of the condition. [4] Last updated: 5/22/2017 A diagnosis of OMS is mostly based on the presence of the[rarediseases.info.nih.gov] Opsoclonus-myoclonus syndrome is a rare neurologic disorder characterized by multidirectional chaotic eye movements, myoclonus in the limbs, and ataxia.[ncbi.nlm.nih.gov] Opsoclonus-myoclonus syndrome (OMS) is a rare neurologic disorder characterized by opsoclonus, myoclonus, ataxia and behavioral disturbance.[ncbi.nlm.nih.gov]

    Missing: Disharmonic Maturation of Phalanges and Carpal Bones

Similar symptoms