HYPOPHOSPHATASIA--PERINATAL (LETHAL) AND INFANTILE ONSET TYPES

ALTERNATE NAMES

Alkaline Phosphotase Deficiency; Hypophosphatasia Infantile Onset; Hypophosphatasia Lethal Form; Hypophosphatasia Perinatal Lethal Form; Perinatal Lethal Hypophosphatasia; Perinatal Rathburn Disease; Phosphoethanolaminuria; Rathburn's Disease

DESCRIPTION

Hypophosphatasia is a rare, inherited metabolic disorder that affects the development of bones and teeth. There are several forms of this disorder, with the perinatal (lethal) and infantile onset types being the most severe.

DIAGNOSTIC TESTING, PHYSICAL FINDINGS, AND ICD-9-CM/ICD-10-CM CODING

Diagnostic testing: Diagnostic testing consisting of subnormally low activity of tissue non-specific alkaline phosphatase (TNALP) enzyme in serum; bone imaging of the bones shows severe demineralization, especially in the metaphyses (the wider part at the extremity of the shaft of a long bone).

Physical findings:

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  A near absence of skeletal mineralization;

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  Fractures;

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  Skin-covered spurs of the knees and elbow;

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  Large fontanels (space between the bones of the skull);

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  Shortened bones;

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  Chest deformities;

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  Muscle weakness;

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  Hypercalcemia (higher than normal level of calcium in your blood); and

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  Multiple congenital abnormalities, leading to respiratory failure.

ICD-9: 275.3

ICD-10: E83.3

PROGRESSION

For perinatal (lethal) onset hypophosphatasia, death occurs either in-utero or within the first months of life. Infantile onset hypophosphatasia presents within the first year of life, and has 50% mortality. The cause of death is usually due to respiratory failure. Perinatal (benign) hypophosphatasia type is characterized by prenatal skeletal manifestations that slowly resolve into the milder childhood and adult onset hypophosphatasia types, which have variable clinical courses.

TREATMENT

Currently there is no cure or definitive treatment for this disorder.

SUGGESTED PROGRAMMATIC ASSESSMENT*

Suggested MER for Evaluation:

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  Clinical history and examination that describes the diagnostic features of the impairment;

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  Laboratory testing for identified enzyme changes; or

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  Imaging documenting decreases in bone mineralization.

Suggested Listings for Evaluation:

DETERMINATION

LISTING

REMARKS

Meets

110.08 A

Evaluate the perinatal (lethal) onset type of hypophospatasia under listing 110.08 A.

110.08 B

Evaluate perinatal (benign), child, and adult onset hypophosphatasia types on a case-by-case basis.

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