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Compartment syndrome is a serious condition. [5] Increased pressure in a body compartment can harm blood flow and tissue function. [5] [6] [7] If not treated quickly, it may cause permanent damage. [7] There are two types: acute and chronic. [8] Acute compartment syndrome can lead to a loss of the affected limb due to tissue death. [6] [9]
The most important signs and symptoms of compartment syndrome are observable before actual contracture. What is known as the five Ps of compartment syndrome include: pain, generally the initial symptom, accompanied by pulselessness, pallor, paralysis, and paraesthesias. Pain will likely also increase upon extension of the affected limbs hands ...
Mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH) – also known as mental retardation, X-linked, syndromic, Najm type (MRXSNA); X-linked intellectual deficit, Najm type; intellectual developmental disorder, X-linked, syndromic, Najm type; X-linked intellectual disability–microcephaly–pontocerebellar hypoplasia syndrome; and by variations of these terms ...
Intellectual disability (ID), also known as general learning disability (in the United Kingdom), [3] and formerly mental retardation (in the United States), [4] [5] [6] is a generalized neurodevelopmental disorder characterized by significant impairment in intellectual and adaptive functioning that is first apparent during childhood.
The diagnostic criteria necessary in order to diagnose intellectual disability consists of: A. Deficits in intellectual functions, such as reasoning, problem solving, planning, abstract thinking, and learning. These deficits are confirmed through clinical assessments and individualized standardized tests.
Generally, diseases outlined within the ICD-10 codes F70-F79 within Chapter V: Mental and behavioural disorders should be included in this category. Subcategories This category has the following 7 subcategories, out of 7 total.
Acrocallosal syndrome; Aldred syndrome; Alopecia contractures dwarfism intellectual disability syndrome; Alwadei syndrome; Aortic arch anomaly - peculiar facies - intellectual disability; Arakawa's syndrome II; Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome; Ayazi syndrome
F78.A1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2023 edition of ICD-10-CM F78.A1 became effective on October 1, 2022. This is the American ICD-10-CM version of F78.A1 - other international versions of ICD-10 F78.A1 may differ.