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^⌊Endocrinopathies (Endocrine System Diseases)

^⌊Microcephalic Primordial Dwarfisms

^⌊ Taybi Linder Syndrome
^⌊ Microcephalic Osteodysplastic Primordial Dwarfism Type II
^⌊ Microcephalic Primordial Dwarfism Crachami Type
^⌊ Microcephalic Primordial Dwarfism Toriello Type

Primordial Dwarfisms
^⌊	Seckel Syndromes
^⌊	Silver-Russell Dwarfism (Silver-Russell Syndrome)
^⌊	Meier-Gorlin Syndrome
^⌊	Osteodysplastic Dwarfism Corsello Type
^⌊	Corsello Opitz Syndrome

Microcephalic Primordial Dwarfism

See Also ↔

Aging & Longevity
Welltrients Guide
Wellness
Fitness (Physical Fitness)
Cleanses & Detoxifying

Microcephalic Primordial Dwarfisms

“Microcephalic Primordial Dwarfisms”

Microcephalic Primordial Dwarfism
In our body, the anomaly, Microcephalic Primordial Dwarfism is a primordial dwarfism associated with a microcephaly, indicative to a specific set of signs, symptoms or other health indicators.
In our body, examples of microcephalic primordial dwarfisms include:

microcephalic osteodysplastic primordial dwarfism type I (Taybi Linder syndrome)
microcephalic osteodysplastic primordial dwarfism type II, aka Majewski osteodysplastic primordial dwarfism type II (MOPD II, or MOPD2)
*

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Microcephalic Primordial Dwarfisms

Taybi Linder Syndrome (Osteodysplastic Primordial Dwarfism Type I)

Microcephalic Osteodysplastic Primordial Dwarfism Type II

Microcephalic Primordial Dwarfism Toriello Type

Primordial Microcephalic Dwarfism Crachami Type

“Taybi Linder Syndrome (Osteodysplastic Primordial Dwarfism Type I)”

Microcephalic Osteodysplastic Primordial Dwarfism Type I
In our body, the anomaly of Microcephalic Osteodysplastic Primordial Dwarfism Type I (Taybi Linder syndrome) is a type of primordial dwarfism, indicative to a specific set of signs, symptoms or other health indicators, associated with a health challenge.

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“Microcephalic Osteodysplastic Primordial Dwarfism Type II”
In our body, the anomaly of Microcephalic Osteodysplastic Primordial Dwarfism Type II, aka Majewski osteodysplastic primordial dwarfism type II (MOPD II, or MOPD2), is a type of primordial dwarfism associated with a microcephaly, indicative to a specific set of signs, symptoms or other health indicators.

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“Microcephalic Primordial Dwarfism Toriello Type”
In our body, the anomaly, Microcephalic Primordial Dwarfism Toriello Type is a type of primordial dwarfism with prenatal-onset growth deficiency, microcephaly, cataracts, mental retardation, enamel hypoplasia, immune deficiency, and generalized delay of ossification, indicative to a specific set of signs, symptoms or other health indicators.

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“Primordial Microcephalic Dwarfism Crachami Type”
In our body, the anomaly, Primordial Microcephalic Dwarfism Crachami Type is a type of primordial dwarfism associated with a microcephaly, indicative to a specific set of signs, symptoms or other health indicators.

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References:
Rauch A. et al "Mutations in the pericentrin (PCNT) gene cause primordial dwarfism" Science. 2008 Feb 8;319(5864):816-9
Halder A. et al "Osteodysplastic primordial dwarfism type II with normal intellect but delayed central nervous system myelination" Am J Med Genet. 1998 Oct 30;80(1):12-5
Toriello HV. et al "An apparently new syndrome of microcephalic primordial dwarfism and cataracts" Am J Med Genet. 1986 Sep;25(1):1-8

†The statements on this Web site have not been evaluated by the Food and Drug Administration (FDA). And are not intended to diagnose, treat, cure or prevent disease. The information presented is not intended to replace medical advice or treatment from your own doctor or healthcare provider. Nothing presented here is intended as a substitute for prescription medication or any other medical treatment prescribed by your doctor.

Microcephalic Primordial Dwarfisms

Microcephalic Primordial Dwarfism

Microcephalic Osteodysplastic Primordial Dwarfism Type I

References: